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stat1(s727) (8a1) monoclonal antibody  (Bioss)


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    Structured Review

    Bioss stat1(s727) (8a1) monoclonal antibody
    Stat1(s727) (8a1) Monoclonal Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 93/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bsm+52209r/STAT1(S727)+(8A1)+Monoclonal+Antibody/custom%40bsm-52209r%4010%2E2147%2FJIR%2ES542033
    Average 93 stars, based on 4 article reviews
    stat1(s727) (8a1) monoclonal antibody - by Bioz Stars, 2026-11
    93/100 stars

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    Article Title: Ranitidine as adjuvant regulates macrophage polarization and activates CTL through PI3K-Akt2 signal pathway
    Article Snippet: The following are the primary antibodies used in this experiment: rabbit anti-phospho-PI3K(Ser1070)(1:1500,bs-6417R,Bioss), rabbit anti-PI3K (1:1500,bs-10657R,Bioss), rabbit anti-phospho-Akt2(Ser474) (1:1500,bs4089R,Bioss),rabbit anti-Akt2(1:1500,10724R,Bioss), rabbit anti-phospho-GSK3β(Ser9) (1:750,R22943,ZEN-BIOSCIENCE),rabbit anti-GSK3β(1:750,R22868, ZEN-BIOSCIENCE), rabbit anti-phospho-Dynamin1(1:1500,bs-13039R,Bioss), rabbit anti-Dynamin1(1:1500,bs13038R,Bioss),rabbit anti-phospho-NF-κB p65(Ser536) (1:1500,AF2006,Affinity), rabbit antiNF-κB p65 (1:1500,AF5006,Affinity), rabbit anti-phospho-STAT4(Tyr693)(1:1500;Bioss, bs- 3430R), rabbit anti-STAT4 (1:1500;Bioss, bs- 10023R), rabbit anti-phospho- STAT1(Ser727) (1:750, bsm-52209R), rabbit anti-STAT1(1:1500,bs-1317R).

    Article Title: Ranitidine as an adjuvant regulates macrophage polarization and activates CTLs through the PI3K-Akt2 signaling pathway.
    Article Snippet: Adjuvants are an indispensable component of vaccines, but there are few adjuvants for human vaccines.. H2 receptor blockers, inhibiting gastric acid secretion, have immune enhancement effects.. Ranitidine (RAN) is a water-soluble H2 receptor blocker, and whether it has an immune-enhancing effect is still unknown.



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    IFIT3 knockdown relieved the intestinal inflammatory response and inhibited the activation of the STAT1/2 pathway in DSS-induced UC mice. ( A and B ) Comparison of colon transduction efficacy in mice between intraperitoneal injection of saline and AAV9 using paraffin sections ( A ) and the IVIS Lumina III imaging system ( B ). Scale bar = 100 µm. ( C ) Comparison of colon length between AAV9-shNC- and AAV9-shIFIT3-treated UC mice. ( D ) Weight changes in the two mouse groups. ( E ) Representative images and histological score of H&E staining in colon tissues from the two mouse groups. Scale bar = 100 µm (top) and 25 µm (bottom). ( F ) mRNA levels of IFIT3, TNF-α, IL-1β and IL-6 in colon tissues from the two mouse groups. ( G ) Protein expressions of STAT1, <t>pSTAT1,</t> STAT2, pSTAT2 and IFIT3 in colon tissues from the two mouse groups. Data was presented as mean ± SD (n = 5). * p < 0.05, ** p < 0.01, *** p < 0.001.
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    IFIT3 knockdown relieved the intestinal inflammatory response and inhibited the activation of the STAT1/2 pathway in DSS-induced UC mice. ( A and B ) Comparison of colon transduction efficacy in mice between intraperitoneal injection of saline and AAV9 using paraffin sections ( A ) and the IVIS Lumina III imaging system ( B ). Scale bar = 100 µm. ( C ) Comparison of colon length between AAV9-shNC- and AAV9-shIFIT3-treated UC mice. ( D ) Weight changes in the two mouse groups. ( E ) Representative images and histological score of H&E staining in colon tissues from the two mouse groups. Scale bar = 100 µm (top) and 25 µm (bottom). ( F ) mRNA levels of IFIT3, TNF-α, IL-1β and IL-6 in colon tissues from the two mouse groups. ( G ) Protein expressions of STAT1, <t>pSTAT1,</t> STAT2, pSTAT2 and IFIT3 in colon tissues from the two mouse groups. Data was presented as mean ± SD (n = 5). * p < 0.05, ** p < 0.01, *** p < 0.001.
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    IFIT3 knockdown relieved the intestinal inflammatory response and inhibited the activation of the STAT1/2 pathway in DSS-induced UC mice. ( A and B ) Comparison of colon transduction efficacy in mice between intraperitoneal injection of saline and AAV9 using paraffin sections ( A ) and the IVIS Lumina III imaging system ( B ). Scale bar = 100 µm. ( C ) Comparison of colon length between AAV9-shNC- and AAV9-shIFIT3-treated UC mice. ( D ) Weight changes in the two mouse groups. ( E ) Representative images and histological score of H&E staining in colon tissues from the two mouse groups. Scale bar = 100 µm (top) and 25 µm (bottom). ( F ) mRNA levels of IFIT3, TNF-α, IL-1β and IL-6 in colon tissues from the two mouse groups. ( G ) Protein expressions of STAT1, <t>pSTAT1,</t> STAT2, pSTAT2 and IFIT3 in colon tissues from the two mouse groups. Data was presented as mean ± SD (n = 5). * p < 0.05, ** p < 0.01, *** p < 0.001.
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    Image Search Results


    IFIT3 knockdown relieved the intestinal inflammatory response and inhibited the activation of the STAT1/2 pathway in DSS-induced UC mice. ( A and B ) Comparison of colon transduction efficacy in mice between intraperitoneal injection of saline and AAV9 using paraffin sections ( A ) and the IVIS Lumina III imaging system ( B ). Scale bar = 100 µm. ( C ) Comparison of colon length between AAV9-shNC- and AAV9-shIFIT3-treated UC mice. ( D ) Weight changes in the two mouse groups. ( E ) Representative images and histological score of H&E staining in colon tissues from the two mouse groups. Scale bar = 100 µm (top) and 25 µm (bottom). ( F ) mRNA levels of IFIT3, TNF-α, IL-1β and IL-6 in colon tissues from the two mouse groups. ( G ) Protein expressions of STAT1, pSTAT1, STAT2, pSTAT2 and IFIT3 in colon tissues from the two mouse groups. Data was presented as mean ± SD (n = 5). * p < 0.05, ** p < 0.01, *** p < 0.001.

    Journal: Journal of Inflammation Research

    Article Title: Downregulation of IFIT3 Relieves the Inflammatory Response in Ulcerative Colitis via Selectively Regulating Macrophage M1 Polarization and the STAT1/2 Signaling Pathway

    doi: 10.2147/JIR.S542033

    Figure Lengend Snippet: IFIT3 knockdown relieved the intestinal inflammatory response and inhibited the activation of the STAT1/2 pathway in DSS-induced UC mice. ( A and B ) Comparison of colon transduction efficacy in mice between intraperitoneal injection of saline and AAV9 using paraffin sections ( A ) and the IVIS Lumina III imaging system ( B ). Scale bar = 100 µm. ( C ) Comparison of colon length between AAV9-shNC- and AAV9-shIFIT3-treated UC mice. ( D ) Weight changes in the two mouse groups. ( E ) Representative images and histological score of H&E staining in colon tissues from the two mouse groups. Scale bar = 100 µm (top) and 25 µm (bottom). ( F ) mRNA levels of IFIT3, TNF-α, IL-1β and IL-6 in colon tissues from the two mouse groups. ( G ) Protein expressions of STAT1, pSTAT1, STAT2, pSTAT2 and IFIT3 in colon tissues from the two mouse groups. Data was presented as mean ± SD (n = 5). * p < 0.05, ** p < 0.01, *** p < 0.001.

    Article Snippet: The PVDF membranes were incubated with primary antibodies against IFIT3 (1:3000; #15201-1-AP, Proteintect), STAT1 (1:1000; # R25799 , Zenbio, Chengdu, China), pSTAT1 (1:1000; #bsm-52209R, Bioss, Beijing, China), STAT2 (1:1000; #R381419 Zenbio), pSTAT2 (1:1000; #bs-3428R, Bioss), and GAPDH (1:1000; #GB15002-100, Servicebio) overnight at 4 °C and then incubated with HRP-labeled secondary antibodies at room temperature for 1 hour.

    Techniques: Knockdown, Activation Assay, Comparison, Transduction, Injection, Saline, Imaging, Staining

    IFIT3 knockdown repressed macrophage M1 polarization by inhibiting the STAT1 pathway in vitro. ( A and B ) mRNA and protein levels of IFIT3 in untreated THP‐1 macrophages or treated with 100 ng/mL LPS or 100 ng/mL LPS + 20 ng/mL IFN‐γ or 20 ng/mL IL‐4. ( C ) mRNA levels of IFIT3 in 100 ng/mL LPS-stimulated macrophages treated with siNC or two siRNAs targeting IFIT3 (siIFIT3-1 and siIFIT3-2). ( D ) mRNA levels of TNF-α, IL-1β and IL-6 in 100 ng/mL LPS-stimulated macrophages treated with siNC and siIFIT3-2. ( E ) Protein levels of STAT1, pSTAT1, STAT2, pSTAT2 and IFIT3 in each group. ( F ) Representative gating and the co-expression of CD86 and CD68 in untreated (M0) and 100 ng/mL LPS-stimulated macrophages (M1) by flow cytometry. ( G ) Representative gating and the co-expression of CD68 and CD86 in 100 ng/mL LPS-stimulated macrophages treated with siNC and siIFIT3-2 by flow cytometry. Data was presented as mean ± SD from 3 independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001.

    Journal: Journal of Inflammation Research

    Article Title: Downregulation of IFIT3 Relieves the Inflammatory Response in Ulcerative Colitis via Selectively Regulating Macrophage M1 Polarization and the STAT1/2 Signaling Pathway

    doi: 10.2147/JIR.S542033

    Figure Lengend Snippet: IFIT3 knockdown repressed macrophage M1 polarization by inhibiting the STAT1 pathway in vitro. ( A and B ) mRNA and protein levels of IFIT3 in untreated THP‐1 macrophages or treated with 100 ng/mL LPS or 100 ng/mL LPS + 20 ng/mL IFN‐γ or 20 ng/mL IL‐4. ( C ) mRNA levels of IFIT3 in 100 ng/mL LPS-stimulated macrophages treated with siNC or two siRNAs targeting IFIT3 (siIFIT3-1 and siIFIT3-2). ( D ) mRNA levels of TNF-α, IL-1β and IL-6 in 100 ng/mL LPS-stimulated macrophages treated with siNC and siIFIT3-2. ( E ) Protein levels of STAT1, pSTAT1, STAT2, pSTAT2 and IFIT3 in each group. ( F ) Representative gating and the co-expression of CD86 and CD68 in untreated (M0) and 100 ng/mL LPS-stimulated macrophages (M1) by flow cytometry. ( G ) Representative gating and the co-expression of CD68 and CD86 in 100 ng/mL LPS-stimulated macrophages treated with siNC and siIFIT3-2 by flow cytometry. Data was presented as mean ± SD from 3 independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001.

    Article Snippet: The PVDF membranes were incubated with primary antibodies against IFIT3 (1:3000; #15201-1-AP, Proteintect), STAT1 (1:1000; # R25799 , Zenbio, Chengdu, China), pSTAT1 (1:1000; #bsm-52209R, Bioss, Beijing, China), STAT2 (1:1000; #R381419 Zenbio), pSTAT2 (1:1000; #bs-3428R, Bioss), and GAPDH (1:1000; #GB15002-100, Servicebio) overnight at 4 °C and then incubated with HRP-labeled secondary antibodies at room temperature for 1 hour.

    Techniques: Knockdown, In Vitro, Expressing, Flow Cytometry

    UPA inhibits inflammation by silencing IFIT3 in LPS-stimulated macrophages. ( A ) mRNA levels of IFIT3, TNF-α, IL-1β and IL-6 in 100 ng/mL LPS-stimulated macrophages with untreated or treated with 100 nM and 400 nM UPA. ( B ) Protein levels of STAT1, pSTAT1, STAT2, pSTAT2 and IFIT3 among cell-groups. ( C ) Schematic diagram of relation among UPA, IFIT3 and STAT1/2 pathways. Data was presented as mean ± SD from 3 independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001.

    Journal: Journal of Inflammation Research

    Article Title: Downregulation of IFIT3 Relieves the Inflammatory Response in Ulcerative Colitis via Selectively Regulating Macrophage M1 Polarization and the STAT1/2 Signaling Pathway

    doi: 10.2147/JIR.S542033

    Figure Lengend Snippet: UPA inhibits inflammation by silencing IFIT3 in LPS-stimulated macrophages. ( A ) mRNA levels of IFIT3, TNF-α, IL-1β and IL-6 in 100 ng/mL LPS-stimulated macrophages with untreated or treated with 100 nM and 400 nM UPA. ( B ) Protein levels of STAT1, pSTAT1, STAT2, pSTAT2 and IFIT3 among cell-groups. ( C ) Schematic diagram of relation among UPA, IFIT3 and STAT1/2 pathways. Data was presented as mean ± SD from 3 independent experiments. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001.

    Article Snippet: The PVDF membranes were incubated with primary antibodies against IFIT3 (1:3000; #15201-1-AP, Proteintect), STAT1 (1:1000; # R25799 , Zenbio, Chengdu, China), pSTAT1 (1:1000; #bsm-52209R, Bioss, Beijing, China), STAT2 (1:1000; #R381419 Zenbio), pSTAT2 (1:1000; #bs-3428R, Bioss), and GAPDH (1:1000; #GB15002-100, Servicebio) overnight at 4 °C and then incubated with HRP-labeled secondary antibodies at room temperature for 1 hour.

    Techniques: