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disc1  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology disc1
    (A) Immunolabelling of kalirin in IMR-32 after KALRN RNAi. Scale bar 20 μm. (B) Western blot analysis of kalirin-8 and kalirin-STYV levels in IMR-32 and SK-N-BE(2)c after KALRN RNAi and kalirin-8 levels in IMR32 after KALRN RNAi or additional negative control siRNAs: control siRNA #2, HNRNPK siRNA, and <t>DISC1</t> siRNA. (C) RAC1 activity in IMR-32 and SK-N-BE(2)c cell treated with kalirin-GEF1 inhibitor#1 (10 μM), kalirin-GEF1 inhibitor#2 (5 μM), RHOA inhibitor (3 μM), RAC1 inhibitor (10 μM), or after SOX11 and KALRN RNAi. (D) Kalrn expression in t-SNE-resolved E12.5 and E13.5 sympathetic precursors: sympathoblasts, Schwann cell precursors, bridge population and chromaffin cells . (E) Sequencing electrophoregrams showing 3′-UTR of kalirin-9 isoform (top) and the exon scheme based on the results of sequencing (bottom). Location of stop codon is marked with “-.” (F) KALRN , TRIO , and TIAM expression in SK-N-BE(2)c (left) after RA (10 μM) treatment. x-axis indicate timepoints in hours. Western Blot analysis of kalirin, TRIO, and βIII-tubulin in SK-N-BE2c after 72 h of RA-treatment (top right) and of TRIO and kalirin-8 in IMR-32 and SK-N-BE(2)c after 72 h of RA treatment (bottom right). (G) Cell viability of NB cell lines treated with vehicle, kalirin-GEF1 inhibitor#2, or kalirin-GEF1 inhibitor#1. Values are reported as mean percent ± SD of vehicle-treated control.
    Disc1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/disc1+sirna/DISC-1+siRNA/pmc08017594-424-9-14
    Average 86 stars, based on 3 article reviews
    disc1 - by Bioz Stars, 2026-09
    86/100 stars

    Images

    1) Product Images from "Kalirin-RAC controls nucleokinetic migration in ADRN-type neuroblastoma"

    Article Title: Kalirin-RAC controls nucleokinetic migration in ADRN-type neuroblastoma

    Journal: Life Science Alliance

    doi: 10.26508/lsa.201900332

    (A) Immunolabelling of kalirin in IMR-32 after KALRN RNAi. Scale bar 20 μm. (B) Western blot analysis of kalirin-8 and kalirin-STYV levels in IMR-32 and SK-N-BE(2)c after KALRN RNAi and kalirin-8 levels in IMR32 after KALRN RNAi or additional negative control siRNAs: control siRNA #2, HNRNPK siRNA, and DISC1 siRNA. (C) RAC1 activity in IMR-32 and SK-N-BE(2)c cell treated with kalirin-GEF1 inhibitor#1 (10 μM), kalirin-GEF1 inhibitor#2 (5 μM), RHOA inhibitor (3 μM), RAC1 inhibitor (10 μM), or after SOX11 and KALRN RNAi. (D) Kalrn expression in t-SNE-resolved E12.5 and E13.5 sympathetic precursors: sympathoblasts, Schwann cell precursors, bridge population and chromaffin cells . (E) Sequencing electrophoregrams showing 3′-UTR of kalirin-9 isoform (top) and the exon scheme based on the results of sequencing (bottom). Location of stop codon is marked with “-.” (F) KALRN , TRIO , and TIAM expression in SK-N-BE(2)c (left) after RA (10 μM) treatment. x-axis indicate timepoints in hours. Western Blot analysis of kalirin, TRIO, and βIII-tubulin in SK-N-BE2c after 72 h of RA-treatment (top right) and of TRIO and kalirin-8 in IMR-32 and SK-N-BE(2)c after 72 h of RA treatment (bottom right). (G) Cell viability of NB cell lines treated with vehicle, kalirin-GEF1 inhibitor#2, or kalirin-GEF1 inhibitor#1. Values are reported as mean percent ± SD of vehicle-treated control.
    Figure Legend Snippet: (A) Immunolabelling of kalirin in IMR-32 after KALRN RNAi. Scale bar 20 μm. (B) Western blot analysis of kalirin-8 and kalirin-STYV levels in IMR-32 and SK-N-BE(2)c after KALRN RNAi and kalirin-8 levels in IMR32 after KALRN RNAi or additional negative control siRNAs: control siRNA #2, HNRNPK siRNA, and DISC1 siRNA. (C) RAC1 activity in IMR-32 and SK-N-BE(2)c cell treated with kalirin-GEF1 inhibitor#1 (10 μM), kalirin-GEF1 inhibitor#2 (5 μM), RHOA inhibitor (3 μM), RAC1 inhibitor (10 μM), or after SOX11 and KALRN RNAi. (D) Kalrn expression in t-SNE-resolved E12.5 and E13.5 sympathetic precursors: sympathoblasts, Schwann cell precursors, bridge population and chromaffin cells . (E) Sequencing electrophoregrams showing 3′-UTR of kalirin-9 isoform (top) and the exon scheme based on the results of sequencing (bottom). Location of stop codon is marked with “-.” (F) KALRN , TRIO , and TIAM expression in SK-N-BE(2)c (left) after RA (10 μM) treatment. x-axis indicate timepoints in hours. Western Blot analysis of kalirin, TRIO, and βIII-tubulin in SK-N-BE2c after 72 h of RA-treatment (top right) and of TRIO and kalirin-8 in IMR-32 and SK-N-BE(2)c after 72 h of RA treatment (bottom right). (G) Cell viability of NB cell lines treated with vehicle, kalirin-GEF1 inhibitor#2, or kalirin-GEF1 inhibitor#1. Values are reported as mean percent ± SD of vehicle-treated control.

    Techniques Used: Western Blot, Negative Control, Control, Activity Assay, Expressing, Sequencing

    Related Articles

    Transfection:

    Article Title: Hypoxic preconditioning decreases nuclear factor κB activity via Disrupted in Schizophrenia-1.
    Article Snippet: Nuclear factor B is a key mediator of inflammation during conditions of hypoxia.. Here, we used models of hypoxic pre-conditioning as mechanism to decrease nuclear factor B activity induced by hypoxia.. Our initial studies suggested that Disrupted in Schizophrenia-1 may be induced by hypoxic pre-conditioning and possibly involved in the regulation of nuclear factor B.

    Article Title: Opposing Actions of the Synapse Associated Protein of 97 kDa Molecular Weight (SAP97) and Disrupted in Schizophrenia 1 (DISC1) on Wnt/β-catenin Signaling
    Article Snippet: .. DISC1 siRNA was purchased from Santa Cruz Luciferase Assay HEK293 cells growing in 60mm dishes were transfected overnight with 50ng of pRL-SV40, 1ug of M50 Super 8× TOPflash, and 4ug of the plasmid of interest (or 2ug + 2ug for epistasis experiments) using Lipofectamine 2000 overnight. .. The following day 60mm dishes were trypsinized and replated into 96 well format (Nunc black microwell SI) in media containing 450ng/ml Wnt3a (R&D Systems) or vehicle.

    Control:

    Article Title: Hypoxic preconditioning decreases nuclear factor κB activity via Disrupted in Schizophrenia-1.
    Article Snippet: Nuclear factor B is a key mediator of inflammation during conditions of hypoxia.. Here, we used models of hypoxic pre-conditioning as mechanism to decrease nuclear factor B activity induced by hypoxia.. Our initial studies suggested that Disrupted in Schizophrenia-1 may be induced by hypoxic pre-conditioning and possibly involved in the regulation of nuclear factor B.

    Luciferase:

    Article Title: Opposing Actions of the Synapse Associated Protein of 97 kDa Molecular Weight (SAP97) and Disrupted in Schizophrenia 1 (DISC1) on Wnt/β-catenin Signaling
    Article Snippet: .. DISC1 siRNA was purchased from Santa Cruz Luciferase Assay HEK293 cells growing in 60mm dishes were transfected overnight with 50ng of pRL-SV40, 1ug of M50 Super 8× TOPflash, and 4ug of the plasmid of interest (or 2ug + 2ug for epistasis experiments) using Lipofectamine 2000 overnight. .. The following day 60mm dishes were trypsinized and replated into 96 well format (Nunc black microwell SI) in media containing 450ng/ml Wnt3a (R&D Systems) or vehicle.

    Plasmid Preparation:

    Article Title: Opposing Actions of the Synapse Associated Protein of 97 kDa Molecular Weight (SAP97) and Disrupted in Schizophrenia 1 (DISC1) on Wnt/β-catenin Signaling
    Article Snippet: .. DISC1 siRNA was purchased from Santa Cruz Luciferase Assay HEK293 cells growing in 60mm dishes were transfected overnight with 50ng of pRL-SV40, 1ug of M50 Super 8× TOPflash, and 4ug of the plasmid of interest (or 2ug + 2ug for epistasis experiments) using Lipofectamine 2000 overnight. .. The following day 60mm dishes were trypsinized and replated into 96 well format (Nunc black microwell SI) in media containing 450ng/ml Wnt3a (R&D Systems) or vehicle.



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    (A) Immunolabelling of kalirin in IMR-32 after KALRN RNAi. Scale bar 20 μm. (B) Western blot analysis of kalirin-8 and kalirin-STYV levels in IMR-32 and SK-N-BE(2)c after KALRN RNAi and kalirin-8 levels in IMR32 after KALRN RNAi or additional negative control siRNAs: control siRNA #2, HNRNPK siRNA, and <t>DISC1</t> siRNA. (C) RAC1 activity in IMR-32 and SK-N-BE(2)c cell treated with kalirin-GEF1 inhibitor#1 (10 μM), kalirin-GEF1 inhibitor#2 (5 μM), RHOA inhibitor (3 μM), RAC1 inhibitor (10 μM), or after SOX11 and KALRN RNAi. (D) Kalrn expression in t-SNE-resolved E12.5 and E13.5 sympathetic precursors: sympathoblasts, Schwann cell precursors, bridge population and chromaffin cells . (E) Sequencing electrophoregrams showing 3′-UTR of kalirin-9 isoform (top) and the exon scheme based on the results of sequencing (bottom). Location of stop codon is marked with “-.” (F) KALRN , TRIO , and TIAM expression in SK-N-BE(2)c (left) after RA (10 μM) treatment. x-axis indicate timepoints in hours. Western Blot analysis of kalirin, TRIO, and βIII-tubulin in SK-N-BE2c after 72 h of RA-treatment (top right) and of TRIO and kalirin-8 in IMR-32 and SK-N-BE(2)c after 72 h of RA treatment (bottom right). (G) Cell viability of NB cell lines treated with vehicle, kalirin-GEF1 inhibitor#2, or kalirin-GEF1 inhibitor#1. Values are reported as mean percent ± SD of vehicle-treated control.
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    Image Search Results


    (A) Immunolabelling of kalirin in IMR-32 after KALRN RNAi. Scale bar 20 μm. (B) Western blot analysis of kalirin-8 and kalirin-STYV levels in IMR-32 and SK-N-BE(2)c after KALRN RNAi and kalirin-8 levels in IMR32 after KALRN RNAi or additional negative control siRNAs: control siRNA #2, HNRNPK siRNA, and DISC1 siRNA. (C) RAC1 activity in IMR-32 and SK-N-BE(2)c cell treated with kalirin-GEF1 inhibitor#1 (10 μM), kalirin-GEF1 inhibitor#2 (5 μM), RHOA inhibitor (3 μM), RAC1 inhibitor (10 μM), or after SOX11 and KALRN RNAi. (D) Kalrn expression in t-SNE-resolved E12.5 and E13.5 sympathetic precursors: sympathoblasts, Schwann cell precursors, bridge population and chromaffin cells . (E) Sequencing electrophoregrams showing 3′-UTR of kalirin-9 isoform (top) and the exon scheme based on the results of sequencing (bottom). Location of stop codon is marked with “-.” (F) KALRN , TRIO , and TIAM expression in SK-N-BE(2)c (left) after RA (10 μM) treatment. x-axis indicate timepoints in hours. Western Blot analysis of kalirin, TRIO, and βIII-tubulin in SK-N-BE2c after 72 h of RA-treatment (top right) and of TRIO and kalirin-8 in IMR-32 and SK-N-BE(2)c after 72 h of RA treatment (bottom right). (G) Cell viability of NB cell lines treated with vehicle, kalirin-GEF1 inhibitor#2, or kalirin-GEF1 inhibitor#1. Values are reported as mean percent ± SD of vehicle-treated control.

    Journal: Life Science Alliance

    Article Title: Kalirin-RAC controls nucleokinetic migration in ADRN-type neuroblastoma

    doi: 10.26508/lsa.201900332

    Figure Lengend Snippet: (A) Immunolabelling of kalirin in IMR-32 after KALRN RNAi. Scale bar 20 μm. (B) Western blot analysis of kalirin-8 and kalirin-STYV levels in IMR-32 and SK-N-BE(2)c after KALRN RNAi and kalirin-8 levels in IMR32 after KALRN RNAi or additional negative control siRNAs: control siRNA #2, HNRNPK siRNA, and DISC1 siRNA. (C) RAC1 activity in IMR-32 and SK-N-BE(2)c cell treated with kalirin-GEF1 inhibitor#1 (10 μM), kalirin-GEF1 inhibitor#2 (5 μM), RHOA inhibitor (3 μM), RAC1 inhibitor (10 μM), or after SOX11 and KALRN RNAi. (D) Kalrn expression in t-SNE-resolved E12.5 and E13.5 sympathetic precursors: sympathoblasts, Schwann cell precursors, bridge population and chromaffin cells . (E) Sequencing electrophoregrams showing 3′-UTR of kalirin-9 isoform (top) and the exon scheme based on the results of sequencing (bottom). Location of stop codon is marked with “-.” (F) KALRN , TRIO , and TIAM expression in SK-N-BE(2)c (left) after RA (10 μM) treatment. x-axis indicate timepoints in hours. Western Blot analysis of kalirin, TRIO, and βIII-tubulin in SK-N-BE2c after 72 h of RA-treatment (top right) and of TRIO and kalirin-8 in IMR-32 and SK-N-BE(2)c after 72 h of RA treatment (bottom right). (G) Cell viability of NB cell lines treated with vehicle, kalirin-GEF1 inhibitor#2, or kalirin-GEF1 inhibitor#1. Values are reported as mean percent ± SD of vehicle-treated control.

    Article Snippet: KALRN (sc-18592), LIS1 (sc-35814), DCX (sc-35214), HNRNPK (sc-38282), and DISC1 (sc-60539) were purchased from Santa Cruz Biotechnologies.

    Techniques: Western Blot, Negative Control, Control, Activity Assay, Expressing, Sequencing

    DISC1 and PCNA levels in eight paired NSCLC tumor (T) and adjacent non-tumor (N) tissues as shown by western blot analysis (A) GAPDH was used as a loading control. DISC1 (B) and PCNA (C) levels were analyzed in tumor tissues (normalized to GAPDH). * P <0.05, compared with adjacent non-tumor tissues. DISC1 expression in NSCLC cell lines (A549, H1299, and SPCA-1) as shown by western blot analysis (D) GAPDH was used as a loading control. DISC1levels were analyzed in NSCLC cell lines (normalized to GAPDH) (E).

    Journal: Oncotarget

    Article Title: DISC1 overexpression promotes non-small cell lung cancer cell proliferation

    doi: 10.18632/oncotarget.18055

    Figure Lengend Snippet: DISC1 and PCNA levels in eight paired NSCLC tumor (T) and adjacent non-tumor (N) tissues as shown by western blot analysis (A) GAPDH was used as a loading control. DISC1 (B) and PCNA (C) levels were analyzed in tumor tissues (normalized to GAPDH). * P <0.05, compared with adjacent non-tumor tissues. DISC1 expression in NSCLC cell lines (A549, H1299, and SPCA-1) as shown by western blot analysis (D) GAPDH was used as a loading control. DISC1levels were analyzed in NSCLC cell lines (normalized to GAPDH) (E).

    Article Snippet: siRNAs targeting DISC1 and negative control siRNA (NC-siRNA) were purchased from GenePharma Co., Ltd (China) (Table ), and a DISC1 over-expression plasmid (DISC1-Flag) (GeneCopoeia, China) was also used. siRNAs and plasmid were transfected into NSCLC cell lines using Lipofectamine 2000 (Life Technologies, USA) according to the manufacturer’s instructions.

    Techniques: Western Blot, Control, Expressing

    IHC staining of DISC1 (A) , p-GSK3β (B) , β-catenin (C) , Cyclin D1 (D) , and Ki-67 (E) in well- (1), moderately- (2), and poorly-differentiated (3) NSCLC tissues (200×).

    Journal: Oncotarget

    Article Title: DISC1 overexpression promotes non-small cell lung cancer cell proliferation

    doi: 10.18632/oncotarget.18055

    Figure Lengend Snippet: IHC staining of DISC1 (A) , p-GSK3β (B) , β-catenin (C) , Cyclin D1 (D) , and Ki-67 (E) in well- (1), moderately- (2), and poorly-differentiated (3) NSCLC tissues (200×).

    Article Snippet: siRNAs targeting DISC1 and negative control siRNA (NC-siRNA) were purchased from GenePharma Co., Ltd (China) (Table ), and a DISC1 over-expression plasmid (DISC1-Flag) (GeneCopoeia, China) was also used. siRNAs and plasmid were transfected into NSCLC cell lines using Lipofectamine 2000 (Life Technologies, USA) according to the manufacturer’s instructions.

    Techniques: Immunohistochemistry

    DISC1 expression correlated with that of p-GSK3β (A) , β-catenin (B) , Cyclin D1 (C) , and Ki-67 (D) .

    Journal: Oncotarget

    Article Title: DISC1 overexpression promotes non-small cell lung cancer cell proliferation

    doi: 10.18632/oncotarget.18055

    Figure Lengend Snippet: DISC1 expression correlated with that of p-GSK3β (A) , β-catenin (B) , Cyclin D1 (C) , and Ki-67 (D) .

    Article Snippet: siRNAs targeting DISC1 and negative control siRNA (NC-siRNA) were purchased from GenePharma Co., Ltd (China) (Table ), and a DISC1 over-expression plasmid (DISC1-Flag) (GeneCopoeia, China) was also used. siRNAs and plasmid were transfected into NSCLC cell lines using Lipofectamine 2000 (Life Technologies, USA) according to the manufacturer’s instructions.

    Techniques: Expressing

    Associations between  DISC1  expression and NSCLC patient clinicopathological parameters

    Journal: Oncotarget

    Article Title: DISC1 overexpression promotes non-small cell lung cancer cell proliferation

    doi: 10.18632/oncotarget.18055

    Figure Lengend Snippet: Associations between DISC1 expression and NSCLC patient clinicopathological parameters

    Article Snippet: siRNAs targeting DISC1 and negative control siRNA (NC-siRNA) were purchased from GenePharma Co., Ltd (China) (Table ), and a DISC1 over-expression plasmid (DISC1-Flag) (GeneCopoeia, China) was also used. siRNAs and plasmid were transfected into NSCLC cell lines using Lipofectamine 2000 (Life Technologies, USA) according to the manufacturer’s instructions.

    Techniques: Expressing

    Univariate analysis of NSCLC patient clinicopathological parameters with respect to survival

    Journal: Oncotarget

    Article Title: DISC1 overexpression promotes non-small cell lung cancer cell proliferation

    doi: 10.18632/oncotarget.18055

    Figure Lengend Snippet: Univariate analysis of NSCLC patient clinicopathological parameters with respect to survival

    Article Snippet: siRNAs targeting DISC1 and negative control siRNA (NC-siRNA) were purchased from GenePharma Co., Ltd (China) (Table ), and a DISC1 over-expression plasmid (DISC1-Flag) (GeneCopoeia, China) was also used. siRNAs and plasmid were transfected into NSCLC cell lines using Lipofectamine 2000 (Life Technologies, USA) according to the manufacturer’s instructions.

    Techniques: Expressing

    Cox regression analysis of potential prognostic factors with respect to NSCLC patient survival

    Journal: Oncotarget

    Article Title: DISC1 overexpression promotes non-small cell lung cancer cell proliferation

    doi: 10.18632/oncotarget.18055

    Figure Lengend Snippet: Cox regression analysis of potential prognostic factors with respect to NSCLC patient survival

    Article Snippet: siRNAs targeting DISC1 and negative control siRNA (NC-siRNA) were purchased from GenePharma Co., Ltd (China) (Table ), and a DISC1 over-expression plasmid (DISC1-Flag) (GeneCopoeia, China) was also used. siRNAs and plasmid were transfected into NSCLC cell lines using Lipofectamine 2000 (Life Technologies, USA) according to the manufacturer’s instructions.

    Techniques: Expressing

    Cumulative overall NSCLC patient survival rate was associated with high (green line) or low (blue line) DISC1 expression.

    Journal: Oncotarget

    Article Title: DISC1 overexpression promotes non-small cell lung cancer cell proliferation

    doi: 10.18632/oncotarget.18055

    Figure Lengend Snippet: Cumulative overall NSCLC patient survival rate was associated with high (green line) or low (blue line) DISC1 expression.

    Article Snippet: siRNAs targeting DISC1 and negative control siRNA (NC-siRNA) were purchased from GenePharma Co., Ltd (China) (Table ), and a DISC1 over-expression plasmid (DISC1-Flag) (GeneCopoeia, China) was also used. siRNAs and plasmid were transfected into NSCLC cell lines using Lipofectamine 2000 (Life Technologies, USA) according to the manufacturer’s instructions.

    Techniques: Expressing

    DISC1 was silenced using siRNAs (DISC1-siRNA1, DISC1-siRNA2 and DISC1-siRNA3) in A549 cells, as detected by western blotting (A) DISC1 knockdown by DISC1-siRNA1, DISC1-siRNA2, and DISC1-siRNA3 (B) PCNA and Cyclin D1 levels were detected by western blotting (C) DISC1-siRNA2-treated A549 cell proliferation as measured by CCK-8 assay (D) Colony formation by DISC1-siRNA2-treated A549 cells (E) The number of cell clones by DIC1-siRNA2-treated A549 cells (F) * P <0.05 compared NC-siRNA-treated cells.

    Journal: Oncotarget

    Article Title: DISC1 overexpression promotes non-small cell lung cancer cell proliferation

    doi: 10.18632/oncotarget.18055

    Figure Lengend Snippet: DISC1 was silenced using siRNAs (DISC1-siRNA1, DISC1-siRNA2 and DISC1-siRNA3) in A549 cells, as detected by western blotting (A) DISC1 knockdown by DISC1-siRNA1, DISC1-siRNA2, and DISC1-siRNA3 (B) PCNA and Cyclin D1 levels were detected by western blotting (C) DISC1-siRNA2-treated A549 cell proliferation as measured by CCK-8 assay (D) Colony formation by DISC1-siRNA2-treated A549 cells (E) The number of cell clones by DIC1-siRNA2-treated A549 cells (F) * P <0.05 compared NC-siRNA-treated cells.

    Article Snippet: siRNAs targeting DISC1 and negative control siRNA (NC-siRNA) were purchased from GenePharma Co., Ltd (China) (Table ), and a DISC1 over-expression plasmid (DISC1-Flag) (GeneCopoeia, China) was also used. siRNAs and plasmid were transfected into NSCLC cell lines using Lipofectamine 2000 (Life Technologies, USA) according to the manufacturer’s instructions.

    Techniques: Western Blot, Knockdown, CCK-8 Assay, Clone Assay

    After DISC1 inhibition or upregulation in A549 cells using DISC1-siRNA2 or DISC1-Flag, respectively, DISC1, p-GSK3β, β-catenin, and cyclin D1 were detected via western blotting.

    Journal: Oncotarget

    Article Title: DISC1 overexpression promotes non-small cell lung cancer cell proliferation

    doi: 10.18632/oncotarget.18055

    Figure Lengend Snippet: After DISC1 inhibition or upregulation in A549 cells using DISC1-siRNA2 or DISC1-Flag, respectively, DISC1, p-GSK3β, β-catenin, and cyclin D1 were detected via western blotting.

    Article Snippet: siRNAs targeting DISC1 and negative control siRNA (NC-siRNA) were purchased from GenePharma Co., Ltd (China) (Table ), and a DISC1 over-expression plasmid (DISC1-Flag) (GeneCopoeia, China) was also used. siRNAs and plasmid were transfected into NSCLC cell lines using Lipofectamine 2000 (Life Technologies, USA) according to the manufacturer’s instructions.

    Techniques: Inhibition, Western Blot

    Hypothesized mechanism for DISC1 overexpression promotion of NSCLC cell proliferation

    Journal: Oncotarget

    Article Title: DISC1 overexpression promotes non-small cell lung cancer cell proliferation

    doi: 10.18632/oncotarget.18055

    Figure Lengend Snippet: Hypothesized mechanism for DISC1 overexpression promotion of NSCLC cell proliferation

    Article Snippet: siRNAs targeting DISC1 and negative control siRNA (NC-siRNA) were purchased from GenePharma Co., Ltd (China) (Table ), and a DISC1 over-expression plasmid (DISC1-Flag) (GeneCopoeia, China) was also used. siRNAs and plasmid were transfected into NSCLC cell lines using Lipofectamine 2000 (Life Technologies, USA) according to the manufacturer’s instructions.

    Techniques: Over Expression

     DISC1-targeting  siRNAs

    Journal: Oncotarget

    Article Title: DISC1 overexpression promotes non-small cell lung cancer cell proliferation

    doi: 10.18632/oncotarget.18055

    Figure Lengend Snippet: DISC1-targeting siRNAs

    Article Snippet: siRNAs targeting DISC1 and negative control siRNA (NC-siRNA) were purchased from GenePharma Co., Ltd (China) (Table ), and a DISC1 over-expression plasmid (DISC1-Flag) (GeneCopoeia, China) was also used. siRNAs and plasmid were transfected into NSCLC cell lines using Lipofectamine 2000 (Life Technologies, USA) according to the manufacturer’s instructions.

    Techniques: Sequencing