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lasp1 antibody  (Proteintech)


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    Structured Review

    Proteintech lasp1 antibody
    (A) Schematic illustration depicting the involvement of PANoptosis in ALI/ARDS pathogenesis in mouse models and clinical samples. (B) Schematic representation of TPNs/Sal B synthesis. (C) Mechanistic diagram of TPNs/Sal B-mediated inhibition of various cell death pathways. (D) Schematic illustrating the role of TPNs/Sal B in maintaining lung epithelial barrier function through the regulation of <t>LASP1.</t> Created in BioRender. Cui, Y. (2026) https://BioRender.com/t11k604 .
    Lasp1 Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 32 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lasp1/LASP1+Antibody/pmc12813356-62-62-65
    Average 93 stars, based on 32 article reviews
    lasp1 antibody - by Bioz Stars, 2026-09
    93/100 stars

    Images

    1) Product Images from "Treating acute respiratory distress syndrome with a multifaceted nanomedicine: Inhibition of PANoptosis and enhancement of lung barrier integrity"

    Article Title: Treating acute respiratory distress syndrome with a multifaceted nanomedicine: Inhibition of PANoptosis and enhancement of lung barrier integrity

    Journal: Materials Today Bio

    doi: 10.1016/j.mtbio.2025.102748

    (A) Schematic illustration depicting the involvement of PANoptosis in ALI/ARDS pathogenesis in mouse models and clinical samples. (B) Schematic representation of TPNs/Sal B synthesis. (C) Mechanistic diagram of TPNs/Sal B-mediated inhibition of various cell death pathways. (D) Schematic illustrating the role of TPNs/Sal B in maintaining lung epithelial barrier function through the regulation of LASP1. Created in BioRender. Cui, Y. (2026) https://BioRender.com/t11k604 .
    Figure Legend Snippet: (A) Schematic illustration depicting the involvement of PANoptosis in ALI/ARDS pathogenesis in mouse models and clinical samples. (B) Schematic representation of TPNs/Sal B synthesis. (C) Mechanistic diagram of TPNs/Sal B-mediated inhibition of various cell death pathways. (D) Schematic illustrating the role of TPNs/Sal B in maintaining lung epithelial barrier function through the regulation of LASP1. Created in BioRender. Cui, Y. (2026) https://BioRender.com/t11k604 .

    Techniques Used: Inhibition

    TPNs/Sal B Improves Lung Epithelial Barrier Function in ALI Mice Through Upregulation of LASP1. (A) Plasma LASP1 levels in clinical ARDS patients compared to healthy controls (HC) (n = 16). (B) Plasma LASP1 levels in LPS-induced ALI mice (n = 8). (C) Plasma LASP1 levels in E protein-induced ALI mice (n = 8). (D) LASP1 protein levels in lung tissue from LPS or E protein-induced ALI mice (n = 6). (E) LASP1 mRNA levels in lung tissue from LPS-induced ALI mice (n = 8). (F) LASP1 mRNA levels in lung tissue from E protein-induced ALI mice (n = 8). (G–J) Correlation of Claudin-4 (G), Claudin-18 (H), Occludin (I), ZO-1 (J) with LASP1 protein expression (n = 30). Data are presented as mean ± SEM. Statistical significance was determined by t -test in A, by one-way ANOVA in B–F and by Pearson correlation analysis in G–J; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001.
    Figure Legend Snippet: TPNs/Sal B Improves Lung Epithelial Barrier Function in ALI Mice Through Upregulation of LASP1. (A) Plasma LASP1 levels in clinical ARDS patients compared to healthy controls (HC) (n = 16). (B) Plasma LASP1 levels in LPS-induced ALI mice (n = 8). (C) Plasma LASP1 levels in E protein-induced ALI mice (n = 8). (D) LASP1 protein levels in lung tissue from LPS or E protein-induced ALI mice (n = 6). (E) LASP1 mRNA levels in lung tissue from LPS-induced ALI mice (n = 8). (F) LASP1 mRNA levels in lung tissue from E protein-induced ALI mice (n = 8). (G–J) Correlation of Claudin-4 (G), Claudin-18 (H), Occludin (I), ZO-1 (J) with LASP1 protein expression (n = 30). Data are presented as mean ± SEM. Statistical significance was determined by t -test in A, by one-way ANOVA in B–F and by Pearson correlation analysis in G–J; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001.

    Techniques Used: Clinical Proteomics, Expressing

    Related Articles

    Control:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
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    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    RNA Sequencing:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Knockdown:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    ChIP-sequencing:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Expressing:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Quantitative RT-PCR:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    ChIP-qPCR:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Binding Assay:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Luciferase:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Phospho-proteomics:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Incubation:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Marker:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Immunofluorescence:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Microscopy:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Transfection:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Immunoprecipitation:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Fractionation:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Co-Immunoprecipitation Assay:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Western Blot:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Negative Control:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Purification:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Over Expression:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Ubiquitin Proteomics:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Cloning:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Mutagenesis:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Generated:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Pull Down Assay:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Infection:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    CCK-8 Assay:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Transwell Assay:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Angiogenesis Assay:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Migration:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Selection:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Xenograft Assay:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).

    Sequencing:

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway.
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: NAT10 promotes the progression of clear cell renal cell carcinoma by regulating ac4C acetylation of NFE2L3 and activating AKT/GSK3β signaling pathway
    Article Snippet: The antigen-antibody reaction was observed by enhanced chemiluminescence.The antigen-antibody reaction was observed by enhanced chemiluminescence.. The antibodies against the following proteins were used: Anti-NAT10 (ab194297, Abcam), NFE2L3 (A15761, ABclonal), HIF1 alpha (340462, ZENBIO), GAPDH (abs132004, Absin), Flag (F1804, Sigma), LASP1 (10515-1-AP, Proteintech), AKT (YT0185, Immunoway), pAKT (YP0006, Immunoway), GSK3β (GB11099, Servicebio), pGSK3β (YP0124, Immunoway), and β- catenin (8480S, CST).

    Article Title: LASP1 in the nucleus accumbens modulates methamphetamine-induced conditioned place preference in mice.
    Article Snippet: Abstract: Methamphetamine (METH) is a highly addictive and widely abused drug that causes complex adaptive changes in the brain’s reward system, such as the nucleus accumbens (NAc).. LASP1 (LIM and SH 3 domain protein 1) as an actin-binding protein, regulates synaptic plasticity.. However, the role and mechanism by which NAc LASP1 contributes to METH addiction remains unclear.

    Article Title: Inhibition of GLUD1 mediated by LASP1 and SYVN1 contributes to hepatitis B virus X protein-induced hepatocarcinogenesis
    Article Snippet: Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).Antibodies targeting mTOR, COXIV, and p-mTOR were obtained from AbClonal (Wuhan, China).. The antibodies against IL-32, SYVN1, AKT, PDK2, LASP1, and GLUD1 were purchased from Proteintech (Wuhan, China).. PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).PI3-K pathway activator SC79 (SF2730) and its inhibitor LY294002 (S1737) were obtained from Beyotime (Shanghai, China).

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization.
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phosphoJAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phosphoERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: RNA-binding protein CCDC137 activates AKT signaling and promotes hepatocellular carcinoma through a novel non-canonical role of DGCR8 in mRNA localization
    Article Snippet: The next day, after three times washing, membranes were incubated with secondary antibodies (diluted at 1:5000 with primary antibody dilution) at room temperature for 1 h. Immunoreactivities were determined using WesternBright ECL Western blotting detection kit (Advansta).. The following antibodies were used in this study: Vinculin (Proteintech, 26520-1-AP, 1:1000 dilution), CCDC137 (Proteintech, 27201–1-AP, 1:1000 dilution), JAK1 (Cell Signaling Technology, #3332, 1:1000 dilution), phospho-JAK1 (Cell Signaling Technology, #3331, 1:1000 dilution), STAT1 (Abcam, ab31369, 1:1000 dilution), phospho Y701-STAT1 (Abcam, ab30645, 1:1000 dilution), STAT3 (Cell Signaling Technology, #12640, 1:1000 dilution), phospho Tyr705-STAT3 (Cell Signaling Technology, #9145, 1:1000 dilution), GSK3β (Cell Signaling Technology, #5676, 1:1000 dilution), phospho-GSK3β (Cell Signaling Technology, #5558, 1:1000 dilution), ERK (Cell Signaling Technology, #4695, 1:4000 dilution), phospho-ERK (Cell Signaling Technology, #4370, 1:4000 dilution), S6K (Cell Signaling Technology, #9262, 1:1000 dilution), phospho-S6K (Santa Cruz, sc-8418, 1:1000 dilution), S6 (Cell Signaling Technology, #2217, 1:2000 dilution), phospho-S6 (Cell Signaling Technology, #5364, 1:2000 dilution), JNK (Cell Signaling Technology, #9252, 1:2000 dilution), phospho-JNK (Cell Signaling Technology, #9251, 1:2000 dilution), YAP (Cell Signaling Technology, #14074, 1:1000 dilution), phospho-YAP (Cell Signaling Technology, #4911, 1:1000 dilution), AKT (Cell Signaling Technology, #4691, 1:1000 dilution), Ser473 phospho-AKT (Santa Cruz, sc-7985, 1:1000 dilution), Thr308 phospho-AKT (Cell Signaling Technology, #4056, 1:1000 dilution), Lamin A/C (Cell Signaling Technology, #2032, 1:1000 dilution), GFP (ABclonal, AE011, 1:4000 dilution), FOXM1 (Proteintech, 13147-1-AP, 1:1000 dilution), JTV1 (Proteintech, 10424-1-AP, 1:1000 dilution), LASP1 (Proteintech, 10515-1-AP, 1:1000 dilution), FLOT2 (Proteintech, 28208-1-AP, 1:1000 dilution), DGCR8 (Proteintech, 10996-1-AP, 1:1000 dilution), β-actin (Bioworld, AP0060, 1:1000 dilution), Flag (Sigma, F1804, 1:1000 dilution), V5 (Sigma, V8012, 1:1000 dilution).. Secondary antibodies for Rabbit (#7074 s, 1:5000) and Mouse (#7076 s, 1:5000) were obtained from Cell Signaling Technology.

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs.
    Article Snippet: The sequence of siRNA and shRNA was provided in the Table S1.of siRNA and shRNA was provided in the Table S1. ... Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).. Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay The cells were harvested and lyzed.Co-immunoprecipitation (Co-IP), Western blot analysis and Glutathione S-transferase pull-down assay..

    Article Title: TRIM15 forms a regulatory loop with the AKT/FOXO1 axis and LASP1 to modulate the sensitivity of HCC cells to TKIs
    Article Snippet: sequence of siRNA and shRNA was provided in the Table . .. Antibodies used as follows: Beta Actin (#66009-1-Ig, Proteintech, 1:5000 dilution), TRIM15 (#13623-1-AP, Proteintech, 1:1000 dilution), LASP1 (#68080-1-Ig, Proteintech, 1:1000 dilution), FOXO1 (#2880S, Cell signaling technology,1:500 dilution), PARP1 (#13371-1-AP, Proteintech, 1:1000 dilution), AKT (#bsm-33278M, Bioss antibodies, 1:2000 dilution), S6K1 (#2708, Cell signaling technology,1:1000 dilution), pS6k1-T398 (#9209, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution), Caspase 3 (#19677-1-AP, Proteintech, 1:1000 dilution), pAKT-S473 (#4060S, Cell signaling technology,1:1000 dilution), pAKT-T308 (#13038, Cell signaling technology,1:1000 dilution), cleaved caspase 3 (#9661, Cell signaling technology,1:2000 dilution).



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    Image Search Results


    (A) Schematic illustration depicting the involvement of PANoptosis in ALI/ARDS pathogenesis in mouse models and clinical samples. (B) Schematic representation of TPNs/Sal B synthesis. (C) Mechanistic diagram of TPNs/Sal B-mediated inhibition of various cell death pathways. (D) Schematic illustrating the role of TPNs/Sal B in maintaining lung epithelial barrier function through the regulation of LASP1. Created in BioRender. Cui, Y. (2026) https://BioRender.com/t11k604 .

    Journal: Materials Today Bio

    Article Title: Treating acute respiratory distress syndrome with a multifaceted nanomedicine: Inhibition of PANoptosis and enhancement of lung barrier integrity

    doi: 10.1016/j.mtbio.2025.102748

    Figure Lengend Snippet: (A) Schematic illustration depicting the involvement of PANoptosis in ALI/ARDS pathogenesis in mouse models and clinical samples. (B) Schematic representation of TPNs/Sal B synthesis. (C) Mechanistic diagram of TPNs/Sal B-mediated inhibition of various cell death pathways. (D) Schematic illustrating the role of TPNs/Sal B in maintaining lung epithelial barrier function through the regulation of LASP1. Created in BioRender. Cui, Y. (2026) https://BioRender.com/t11k604 .

    Article Snippet: Dexamethasone (Aladdin), Shikonin (Aladdin), LPS (L2630, sigma), SARS-CoV-2 Envelope Protein (E protein; DRA33, novoprotein), Salvianolic acid B (M4140, Abmole), Protein Extraction Reagent (P0013, Beyotime), Protease and Phosphatase Inhibitor (78442, Thermo), Enhanced BCA Protein Assay Kit (P0010S, Beyotime), SDS-PAGE Gel Kit (CW0022S, CWBIO), GSDMD antibody (A18121, Abclonal), caspase-3 antibody (19677-1-AP, Proteintech), caspase-8 antibody (13423-1-AP, Proteintech), MLKL antibody (66675-1-Ig, Proteintech), Tubulin antibody (66031-1-Ig, Proteintech), LASP1 antibody (10515-1-AP, Proteintech), ZBP1 antibody (sc-271483, Santa Cruz), Mouse TNF-α enzyme-linked immunoassay (ELISA) kit (EMC102a, NeoBioscience), Mouse IL-1β ELISA kit (EMC001b, NeoBioscience), Mouse LASP1 ELISA kit (ZC-55248, ZCIBIO), Human LASP1 ELISA kit (ZC-55237, ZCIBIO), Evans blue (CE5171, Coolaber), 4 % polyformaldehyde (G1101, Servicebio), Trizol (15596026CN, Thermo), HiScript II Q RT SuperMix for qPCR (R223, Vazyme), ChamQ Universal SYBR qPCR Master Mix (Q711-03, Vazyme)

    Techniques: Inhibition

    TPNs/Sal B Improves Lung Epithelial Barrier Function in ALI Mice Through Upregulation of LASP1. (A) Plasma LASP1 levels in clinical ARDS patients compared to healthy controls (HC) (n = 16). (B) Plasma LASP1 levels in LPS-induced ALI mice (n = 8). (C) Plasma LASP1 levels in E protein-induced ALI mice (n = 8). (D) LASP1 protein levels in lung tissue from LPS or E protein-induced ALI mice (n = 6). (E) LASP1 mRNA levels in lung tissue from LPS-induced ALI mice (n = 8). (F) LASP1 mRNA levels in lung tissue from E protein-induced ALI mice (n = 8). (G–J) Correlation of Claudin-4 (G), Claudin-18 (H), Occludin (I), ZO-1 (J) with LASP1 protein expression (n = 30). Data are presented as mean ± SEM. Statistical significance was determined by t -test in A, by one-way ANOVA in B–F and by Pearson correlation analysis in G–J; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001.

    Journal: Materials Today Bio

    Article Title: Treating acute respiratory distress syndrome with a multifaceted nanomedicine: Inhibition of PANoptosis and enhancement of lung barrier integrity

    doi: 10.1016/j.mtbio.2025.102748

    Figure Lengend Snippet: TPNs/Sal B Improves Lung Epithelial Barrier Function in ALI Mice Through Upregulation of LASP1. (A) Plasma LASP1 levels in clinical ARDS patients compared to healthy controls (HC) (n = 16). (B) Plasma LASP1 levels in LPS-induced ALI mice (n = 8). (C) Plasma LASP1 levels in E protein-induced ALI mice (n = 8). (D) LASP1 protein levels in lung tissue from LPS or E protein-induced ALI mice (n = 6). (E) LASP1 mRNA levels in lung tissue from LPS-induced ALI mice (n = 8). (F) LASP1 mRNA levels in lung tissue from E protein-induced ALI mice (n = 8). (G–J) Correlation of Claudin-4 (G), Claudin-18 (H), Occludin (I), ZO-1 (J) with LASP1 protein expression (n = 30). Data are presented as mean ± SEM. Statistical significance was determined by t -test in A, by one-way ANOVA in B–F and by Pearson correlation analysis in G–J; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001.

    Article Snippet: Dexamethasone (Aladdin), Shikonin (Aladdin), LPS (L2630, sigma), SARS-CoV-2 Envelope Protein (E protein; DRA33, novoprotein), Salvianolic acid B (M4140, Abmole), Protein Extraction Reagent (P0013, Beyotime), Protease and Phosphatase Inhibitor (78442, Thermo), Enhanced BCA Protein Assay Kit (P0010S, Beyotime), SDS-PAGE Gel Kit (CW0022S, CWBIO), GSDMD antibody (A18121, Abclonal), caspase-3 antibody (19677-1-AP, Proteintech), caspase-8 antibody (13423-1-AP, Proteintech), MLKL antibody (66675-1-Ig, Proteintech), Tubulin antibody (66031-1-Ig, Proteintech), LASP1 antibody (10515-1-AP, Proteintech), ZBP1 antibody (sc-271483, Santa Cruz), Mouse TNF-α enzyme-linked immunoassay (ELISA) kit (EMC102a, NeoBioscience), Mouse IL-1β ELISA kit (EMC001b, NeoBioscience), Mouse LASP1 ELISA kit (ZC-55248, ZCIBIO), Human LASP1 ELISA kit (ZC-55237, ZCIBIO), Evans blue (CE5171, Coolaber), 4 % polyformaldehyde (G1101, Servicebio), Trizol (15596026CN, Thermo), HiScript II Q RT SuperMix for qPCR (R223, Vazyme), ChamQ Universal SYBR qPCR Master Mix (Q711-03, Vazyme)

    Techniques: Clinical Proteomics, Expressing

    Elevated LASP1 expression in NEPC (A) Schematic summary of identification of five potential early epigenetic drivers of NEPC transdifferentiation. The data were analyzed between PDX Adeno and NEPC, and LTL331 post-castration week 8 compared to pre-castration (Pre-Cx). (B) Heatmap displaying consistent increased expression of five potential early epigenetic drivers in LTL331 post-castration week 8 and week 12 compared to Pre-Cx). (C) Consistent increased expression of LASP1 mRNA in LTL331 post-castration week 6, 8, and 10 compared to Pre-Cx. Data show mean ± SEM from three biological replicates. The p value was calculated with unpaired two-tail Student’s t tests. (D) Representative images of IHC staining of LASP1, CgA, NCAM1, SYP, and AR in adenocarcinoma tumors (Adeno) and neuroendocrine tumors (NEPC) of both clinical samples and PDX samples. (E) Western blot analysis of LASP1, ENO2, and REST expression in Adeno and NEPC PDX samples.

    Journal: Cell Genomics

    Article Title: CXCR4-LASP1-G9a-SNAIL axis drives NEPC transdifferentiation via induction of EMT and downregulation of REST

    doi: 10.1016/j.xgen.2025.100916

    Figure Lengend Snippet: Elevated LASP1 expression in NEPC (A) Schematic summary of identification of five potential early epigenetic drivers of NEPC transdifferentiation. The data were analyzed between PDX Adeno and NEPC, and LTL331 post-castration week 8 compared to pre-castration (Pre-Cx). (B) Heatmap displaying consistent increased expression of five potential early epigenetic drivers in LTL331 post-castration week 8 and week 12 compared to Pre-Cx). (C) Consistent increased expression of LASP1 mRNA in LTL331 post-castration week 6, 8, and 10 compared to Pre-Cx. Data show mean ± SEM from three biological replicates. The p value was calculated with unpaired two-tail Student’s t tests. (D) Representative images of IHC staining of LASP1, CgA, NCAM1, SYP, and AR in adenocarcinoma tumors (Adeno) and neuroendocrine tumors (NEPC) of both clinical samples and PDX samples. (E) Western blot analysis of LASP1, ENO2, and REST expression in Adeno and NEPC PDX samples.

    Article Snippet: Fixed cells were then permeabilized with 0.5% Triton X-100 for 30 min. For the IF, fixed cells were incubated for 1 h in 3%BSA in PBS+0.1% Tween (PBS-T), and incubated overnight at 4°C with primary antibodies, LASP1 (Santa Cruz, 374059) or Snail (Cell signaling, 3879).

    Techniques: Expressing, Immunohistochemistry, Western Blot

    LASP1 drives NE transdifferentiation (A) Real-time qPCR analysis of LASP1 , SYP , ENO2 , and NCAM1 expression in 42D ENZR cells compared to 16D CRPC cells. (B) Western blot analysis of LASP1, SYP, ENO2, and NCAM1 expression in 42D ENZR cells compared to 16D CRPC cells. (C) Real-time qPCR analysis of LASP1 , SYP , ENO2 , and NCAM1 expression in 16D CRPC cells castrated for 3, 7, and 14 days. Cells were cultured in RPMI + 10% fetal bovine serum (FBS), RPMI + 10% charcoal-stripped serum (CSS), or RPMI + 10% CSS+10 μM enzalutamide (ENZ). (D) Western blot analysis of LASP1, SYP, ENO2, and NCAM1 expression in 16D CRPC cells castrated for 3, 7, and 14 days. Cells were cultured in RPMI + 10% FBS, RPMI + 10% CSS, or RPMI + 10% CSS +10 μM ENZ. (E) Western blot analysis of LASP1 levels in LASP1-OE 16D CRPC stable cell lines. (F) Real-time qPCR analysis of SYP , ENO2 , and NCAM1 expression in exogenously expressing vector or LASP1 in 16D CRPC cells. LASP1-OE 16D CRPC or mock-transduced 16D CRPC were cultured in RPMI + 10% FBS, RPMI + 10% CSS, or RPMI + 10% CSS +10 μM ENZ. (G) Western blot analysis of ENO2 and NCAM1 expression in exogenously expressing either mock or LASP1 in 16D CRPC cells. LASP1-OE 16D CRPC or mock-transduced 16D CRPC were cultured in RPMI + 10% FBS, RPMI + 10% CSS, or RPMI + 10% CSS +10 μM ENZ. (H) Representative IHC images of NCAM1, ENO2, AR, and LASP1 and hematoxylin and eosin (H&E) staining for LASP1-OE 16D CRPC or mock-transduced 16D CRPC xenograft tumors. (I) GSEA analysis of LASP1-OE 16D CRPC tumor-derived cells versus mock-transduced 16D CRPC cells. (J) Heatmap displaying increased NE marker expression in LASP1-OE 16D CRPC tumor-derived cells versus mock-transduced 16D CRPC cells. Data show mean ± SEM from three biological replicates. The p values (A and F) were calculated with unpaired two-tail Student’s t tests. Densitometry analysis data are in .

    Journal: Cell Genomics

    Article Title: CXCR4-LASP1-G9a-SNAIL axis drives NEPC transdifferentiation via induction of EMT and downregulation of REST

    doi: 10.1016/j.xgen.2025.100916

    Figure Lengend Snippet: LASP1 drives NE transdifferentiation (A) Real-time qPCR analysis of LASP1 , SYP , ENO2 , and NCAM1 expression in 42D ENZR cells compared to 16D CRPC cells. (B) Western blot analysis of LASP1, SYP, ENO2, and NCAM1 expression in 42D ENZR cells compared to 16D CRPC cells. (C) Real-time qPCR analysis of LASP1 , SYP , ENO2 , and NCAM1 expression in 16D CRPC cells castrated for 3, 7, and 14 days. Cells were cultured in RPMI + 10% fetal bovine serum (FBS), RPMI + 10% charcoal-stripped serum (CSS), or RPMI + 10% CSS+10 μM enzalutamide (ENZ). (D) Western blot analysis of LASP1, SYP, ENO2, and NCAM1 expression in 16D CRPC cells castrated for 3, 7, and 14 days. Cells were cultured in RPMI + 10% FBS, RPMI + 10% CSS, or RPMI + 10% CSS +10 μM ENZ. (E) Western blot analysis of LASP1 levels in LASP1-OE 16D CRPC stable cell lines. (F) Real-time qPCR analysis of SYP , ENO2 , and NCAM1 expression in exogenously expressing vector or LASP1 in 16D CRPC cells. LASP1-OE 16D CRPC or mock-transduced 16D CRPC were cultured in RPMI + 10% FBS, RPMI + 10% CSS, or RPMI + 10% CSS +10 μM ENZ. (G) Western blot analysis of ENO2 and NCAM1 expression in exogenously expressing either mock or LASP1 in 16D CRPC cells. LASP1-OE 16D CRPC or mock-transduced 16D CRPC were cultured in RPMI + 10% FBS, RPMI + 10% CSS, or RPMI + 10% CSS +10 μM ENZ. (H) Representative IHC images of NCAM1, ENO2, AR, and LASP1 and hematoxylin and eosin (H&E) staining for LASP1-OE 16D CRPC or mock-transduced 16D CRPC xenograft tumors. (I) GSEA analysis of LASP1-OE 16D CRPC tumor-derived cells versus mock-transduced 16D CRPC cells. (J) Heatmap displaying increased NE marker expression in LASP1-OE 16D CRPC tumor-derived cells versus mock-transduced 16D CRPC cells. Data show mean ± SEM from three biological replicates. The p values (A and F) were calculated with unpaired two-tail Student’s t tests. Densitometry analysis data are in .

    Article Snippet: Fixed cells were then permeabilized with 0.5% Triton X-100 for 30 min. For the IF, fixed cells were incubated for 1 h in 3%BSA in PBS+0.1% Tween (PBS-T), and incubated overnight at 4°C with primary antibodies, LASP1 (Santa Cruz, 374059) or Snail (Cell signaling, 3879).

    Techniques: Expressing, Western Blot, Cell Culture, Stable Transfection, Plasmid Preparation, Staining, Derivative Assay, Marker

    Inhibition of G9a leads to phenotypic reversion of NEPC (A) Increased LASP1 / UHRF1 / DNMT1 / EHMT2 / SNAI1 gene signature in neuroendocrine tumors (NEPC) compared to adenocarcinoma tumors (Adeno) across VPC PDX models and three clinical cohorts. (B) Representative images of G9a IHC staining in both Adeno and NEPC clinical samples and PDX samples. (C) Representative images of IHC staining of H3K9me1, H3K9me2, and H3K9me3 in Adeno and NEPC clinical samples. (D) ChIP-seq showing H3K9me3-binding intensity reported as fold change over input in LTL331 and LTL331R PDX. (E) ChIP-PCR shows the enrichment of H3K9me3 on the promoters of AR and REST in NEPC LTL352 versus Adeno LTL313B. NC, negative control region. Bar graphs show mean ± SEM. The p values were calculated by unpaired two-tail Student’s t test. (F) Western blot analysis of H3K9me1, H3K9me2, and H3K9me3 in LTL331R-2D cells treated with different concentrations of UNC0642, a G9a inhibitor, for 40 h. Densitometry analysis data are in . (G) RNA expression levels of NE markers and REST in LTL331R-2D cells treated with UNC0642 versus control. (H) Heatmap displaying luminal genes in LTL331R-2D cells treated with UNC0642 versus control. (I) Heatmap displaying stem-like marker genes in LTL331R-2D cells treated with UNC0642 versus control. (J) Heatmap displaying basal marker genes in LTL331R-2D cells treated with UNC0642 versus control. (K) Heatmap displaying EMT marker genes in LTL331R-2D cells treated with UNC0642 versus control. (L) Heatmap displaying Nelson response to androgen up genes in LTL331R-2D cells treated with UNC0642 versus control.

    Journal: Cell Genomics

    Article Title: CXCR4-LASP1-G9a-SNAIL axis drives NEPC transdifferentiation via induction of EMT and downregulation of REST

    doi: 10.1016/j.xgen.2025.100916

    Figure Lengend Snippet: Inhibition of G9a leads to phenotypic reversion of NEPC (A) Increased LASP1 / UHRF1 / DNMT1 / EHMT2 / SNAI1 gene signature in neuroendocrine tumors (NEPC) compared to adenocarcinoma tumors (Adeno) across VPC PDX models and three clinical cohorts. (B) Representative images of G9a IHC staining in both Adeno and NEPC clinical samples and PDX samples. (C) Representative images of IHC staining of H3K9me1, H3K9me2, and H3K9me3 in Adeno and NEPC clinical samples. (D) ChIP-seq showing H3K9me3-binding intensity reported as fold change over input in LTL331 and LTL331R PDX. (E) ChIP-PCR shows the enrichment of H3K9me3 on the promoters of AR and REST in NEPC LTL352 versus Adeno LTL313B. NC, negative control region. Bar graphs show mean ± SEM. The p values were calculated by unpaired two-tail Student’s t test. (F) Western blot analysis of H3K9me1, H3K9me2, and H3K9me3 in LTL331R-2D cells treated with different concentrations of UNC0642, a G9a inhibitor, for 40 h. Densitometry analysis data are in . (G) RNA expression levels of NE markers and REST in LTL331R-2D cells treated with UNC0642 versus control. (H) Heatmap displaying luminal genes in LTL331R-2D cells treated with UNC0642 versus control. (I) Heatmap displaying stem-like marker genes in LTL331R-2D cells treated with UNC0642 versus control. (J) Heatmap displaying basal marker genes in LTL331R-2D cells treated with UNC0642 versus control. (K) Heatmap displaying EMT marker genes in LTL331R-2D cells treated with UNC0642 versus control. (L) Heatmap displaying Nelson response to androgen up genes in LTL331R-2D cells treated with UNC0642 versus control.

    Article Snippet: Fixed cells were then permeabilized with 0.5% Triton X-100 for 30 min. For the IF, fixed cells were incubated for 1 h in 3%BSA in PBS+0.1% Tween (PBS-T), and incubated overnight at 4°C with primary antibodies, LASP1 (Santa Cruz, 374059) or Snail (Cell signaling, 3879).

    Techniques: Inhibition, Immunohistochemistry, ChIP-sequencing, Binding Assay, Negative Control, Western Blot, RNA Expression, Control, Marker

    LASP1 interacting with SNAIL regulates REST expression (A) SNAIL forms a complex with LASP1 as measured by coIP in NCI-H660 cells. (B) Schematic diagram of protein-structure domains of LASP1 and SNAIL constructs. (C) LASP1 forms a complex with SNAIL through LIM domain and SNAG domain, respectively, measured by coIP in 293T cells transfected with mutant constructs. (D) Western blot analysis of phospho-LASP1 in LNCaP cells. LNCaP cells were serum starved overnight, followed by 10 μM forskolin stimulation at different time points. (E) Representative immunofluorescence images of LASP1 in LNCaP cells stimulated with 10 μM forskolin at different time points. (F) Representative immunofluorescence images of LASP1 and SNAIL in LNCaP cells stimulated with 10 μM forskolin at different time points. (G) Representative images of proximity-ligation assay measuring LASP1 and SNAIL interaction in LNCaP cells after forskolin stimulation. (H) Representative images of proximity-ligation assay measuring phospho-LASP1 and SNAIL interaction in LNCaP cells after forskolin stimulation. (I) LASP1 forms a complex with SNAIL, co-occupying E-box motif in the REST promoter region measured by ChIP-PCR. (J) REST promoter luciferase reporter analysis in LNCaP cells with increased doses of ectopic expression of LASP1 or SNAIL. (K) REST promoter luciferase reporter analysis in 293T cells with ectopic expression of LASP1 and SNAIL mutant constructs. (L) Real-time qPCR and western blot analysis of LASP1, REST, and ENO2 expression in NCI-H660 cells transfected with siRNAs against LASP1 or negative-control siRNA. (M) Real-time qPCR and western blot analysis of LASP1, REST, and ENO2 expression in LNCaP transfected with LASP1 or control vector. Data show mean ± SEM from three biological replicates. The p values (G–M) were calculated with unpaired two-tail Student’s t tests. Densitometry analysis data are in .

    Journal: Cell Genomics

    Article Title: CXCR4-LASP1-G9a-SNAIL axis drives NEPC transdifferentiation via induction of EMT and downregulation of REST

    doi: 10.1016/j.xgen.2025.100916

    Figure Lengend Snippet: LASP1 interacting with SNAIL regulates REST expression (A) SNAIL forms a complex with LASP1 as measured by coIP in NCI-H660 cells. (B) Schematic diagram of protein-structure domains of LASP1 and SNAIL constructs. (C) LASP1 forms a complex with SNAIL through LIM domain and SNAG domain, respectively, measured by coIP in 293T cells transfected with mutant constructs. (D) Western blot analysis of phospho-LASP1 in LNCaP cells. LNCaP cells were serum starved overnight, followed by 10 μM forskolin stimulation at different time points. (E) Representative immunofluorescence images of LASP1 in LNCaP cells stimulated with 10 μM forskolin at different time points. (F) Representative immunofluorescence images of LASP1 and SNAIL in LNCaP cells stimulated with 10 μM forskolin at different time points. (G) Representative images of proximity-ligation assay measuring LASP1 and SNAIL interaction in LNCaP cells after forskolin stimulation. (H) Representative images of proximity-ligation assay measuring phospho-LASP1 and SNAIL interaction in LNCaP cells after forskolin stimulation. (I) LASP1 forms a complex with SNAIL, co-occupying E-box motif in the REST promoter region measured by ChIP-PCR. (J) REST promoter luciferase reporter analysis in LNCaP cells with increased doses of ectopic expression of LASP1 or SNAIL. (K) REST promoter luciferase reporter analysis in 293T cells with ectopic expression of LASP1 and SNAIL mutant constructs. (L) Real-time qPCR and western blot analysis of LASP1, REST, and ENO2 expression in NCI-H660 cells transfected with siRNAs against LASP1 or negative-control siRNA. (M) Real-time qPCR and western blot analysis of LASP1, REST, and ENO2 expression in LNCaP transfected with LASP1 or control vector. Data show mean ± SEM from three biological replicates. The p values (G–M) were calculated with unpaired two-tail Student’s t tests. Densitometry analysis data are in .

    Article Snippet: Fixed cells were then permeabilized with 0.5% Triton X-100 for 30 min. For the IF, fixed cells were incubated for 1 h in 3%BSA in PBS+0.1% Tween (PBS-T), and incubated overnight at 4°C with primary antibodies, LASP1 (Santa Cruz, 374059) or Snail (Cell signaling, 3879).

    Techniques: Expressing, Construct, Transfection, Mutagenesis, Western Blot, Immunofluorescence, Proximity Ligation Assay, Luciferase, Negative Control, Control, Plasmid Preparation

    Inhibition of CXCR4 induced phenotypic reversion in NEPC cells (A) Elevated CXCR4 mRNA expression in neuroendocrine tumors (NEPC) from PDX samples and two clinical cohorts. (B) Representative IHC staining of CXCR4 in NEPC tumors of PDX and clinical samples. (C) CXCR4 forms a complex with LASP1 measured by coIP in 16D CRPC cells under serum-starvation conditions. (D) Representative immunofluorescence of LASP1 in 16D CRPC cells stimulated with CXCL12. 16D CRPC cells were serum starved overnight, followed by stimulation of 50 nM CXCL12. (E) Real-time qPCR analysis of NCAM1 and ENO2 in 16D CRPC cells treated with CXCL12. Data show mean ± SEM from three biological replicates. The p values were calculated with unpaired two-tail Student’s t tests. (F) Representative immunofluorescence of LASP1 in 16D CRPC cells stimulated with CXCL12 ± AMD3100. 16D CRPC cells were serum starved overnight, followed by stimulation of 50 nM CXCL12 with or without 5 μg/mL AMD3100. (G) RNA expression levels of NE markers and REST in LTL331R-2D cells treated with AMD3100 versus control. (H) Heatmap displaying luminal genes and Nelson response to androgen up genes in LTL331R-2D cells treated AMD3100 versus control.

    Journal: Cell Genomics

    Article Title: CXCR4-LASP1-G9a-SNAIL axis drives NEPC transdifferentiation via induction of EMT and downregulation of REST

    doi: 10.1016/j.xgen.2025.100916

    Figure Lengend Snippet: Inhibition of CXCR4 induced phenotypic reversion in NEPC cells (A) Elevated CXCR4 mRNA expression in neuroendocrine tumors (NEPC) from PDX samples and two clinical cohorts. (B) Representative IHC staining of CXCR4 in NEPC tumors of PDX and clinical samples. (C) CXCR4 forms a complex with LASP1 measured by coIP in 16D CRPC cells under serum-starvation conditions. (D) Representative immunofluorescence of LASP1 in 16D CRPC cells stimulated with CXCL12. 16D CRPC cells were serum starved overnight, followed by stimulation of 50 nM CXCL12. (E) Real-time qPCR analysis of NCAM1 and ENO2 in 16D CRPC cells treated with CXCL12. Data show mean ± SEM from three biological replicates. The p values were calculated with unpaired two-tail Student’s t tests. (F) Representative immunofluorescence of LASP1 in 16D CRPC cells stimulated with CXCL12 ± AMD3100. 16D CRPC cells were serum starved overnight, followed by stimulation of 50 nM CXCL12 with or without 5 μg/mL AMD3100. (G) RNA expression levels of NE markers and REST in LTL331R-2D cells treated with AMD3100 versus control. (H) Heatmap displaying luminal genes and Nelson response to androgen up genes in LTL331R-2D cells treated AMD3100 versus control.

    Article Snippet: Fixed cells were then permeabilized with 0.5% Triton X-100 for 30 min. For the IF, fixed cells were incubated for 1 h in 3%BSA in PBS+0.1% Tween (PBS-T), and incubated overnight at 4°C with primary antibodies, LASP1 (Santa Cruz, 374059) or Snail (Cell signaling, 3879).

    Techniques: Inhibition, Expressing, Immunohistochemistry, Immunofluorescence, RNA Expression, Control