anti rat cd10 antibody (R&D Systems)
Structured Review

Anti Rat Cd10 Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/neprilysin/Human%2FMouse+Neprilysin%2FCD10+Antibody/pmc12881290-86-8-20
Average 92 stars, based on 7 article reviews
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1) Product Images from "Stimulator of Interferon Genes Is a Fine-Tuner, but Not a Prime Mover, of Kidney Inflammation"
Article Title: Stimulator of Interferon Genes Is a Fine-Tuner, but Not a Prime Mover, of Kidney Inflammation
Journal: The American Journal of Pathology
doi: 10.1016/j.ajpath.2025.10.013
Figure Legend Snippet: Knockout of STING attenuates, but does not negate, inflammatory gene up-regulation induced by double-stranded DNA (dsDNA) in tubule epithelial cells (TECs). A: Dual staining of primary cultured TECs for aquaporin 1 (AQP1; red) and CD10 (green). B: Immunoblotting kidney homogenates of wild-type and STING KO mice showing absence of STING protein in STING KO mice. C: Acrylamide gel showing dsDNA after preparation according to the protocol described previously, and 1 to 3 are replicates. D: Immunoblotting for STING, cGMP-AMP synthase (cGAS), TANK-binding kinase 1 (TBK1) Ser172 phosphorylation (pTBK1), total TBK1, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in control and STING KO TECs transfected with vehicle or 2.5 μg dsDNA for 6 hours E – I: Quantitative real-time RT-PCR for Ifnb1 ( E ), Il6 ( F ), Tnf ( G ), Tgfb1 ( H ), and Havcr1 ( I ) in TECs transfected with vehicle or dsDNA. Values are means ± SD ( D – I ). n = 6 per condition ( D – I ). ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, and ∗∗∗∗ P < 0.0001 by one-way analysis of variance with Tukey post test. Scale bars = 50 μm ( A ).
Techniques Used: Knock-Out, Staining, Cell Culture, Western Blot, Acrylamide Gel Assay, Binding Assay, Phospho-proteomics, Control, Transfection, Quantitative RT-PCR
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