pdl1 fc chimera protein (R&D Systems)
Structured Review

Pdl1 Fc Chimera Protein, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 31 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/recombinant+mouse+b7/Recombinant+Mouse+PD-L1%2FB7-H1+Fc+Chimera+Protein%2C+CF/bio_rxiv__2025__10__19__683142-342-30-34
Average 93 stars, based on 31 article reviews
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1) Product Images from "CD8 T cells mediate immunosurveillance for neoantigen+ epithelial stem cells in the colon"
Article Title: CD8 T cells mediate immunosurveillance for neoantigen+ epithelial stem cells in the colon
Journal: bioRxiv
doi: 10.1101/2025.10.19.683142
Figure Legend Snippet: a , Representative (n = 6) 20x CellDIVE immunofluorescence image from days 6-8. GFP = NINJA and Nur77, pink = PDL1, blue = EpCAM, cyan = CD45, white = EpCAM. b , 48 hour in-vitro stimulation with CD3, CD28 and either PDL1 or an Fc control. Representative histogram expression of Perforin, Granzyme A, and Granzyme B with quantification of the percent expression. c , Ex-vivo GP33 peptide stimulation. Representative IFNγ and TNFα flow plots, pre-gated on CD8+ T cells. d , Quantification of the percent of antigen-specific T cells (GP33 and GP34 tetramer-positive CD8+ T cells) that make IFNγ following GP33 stimulation. e , KEGG IFNγ response module enrichment score. f , CD274 transcript expression. g , UMAP reduction with LGR5 expression and PDL1 expression from healthy control and inflammatory colitis conditions. h , representative histogram of PDL1 expression following a 24-hour in-vitro stimulation of primary human β cells and human small intestine organoids with various doses of IFNγ. I , Quantification of the %PDL1+ human β cells and human small intestine organoids following the IFN γ stimulation. J , Human CD274 promoter methylation across various organs and cell types and mouse CD274 promoter methylation in islets and colonic epithelial cells, three mice each, pooled with two technical replicates. To assess statistical significance of the PDL1 stimulations, a one-way ANOVA with Tukey’s multiple comparison test was performed. To assess the statistical significance of the KEGG IFNγ signature, Wilcoxon sign-rank tests were performed. To determine the statistical significance of the in-vitro IFNγ stimulations, a Mixed-effects model (REML) with Šídák’s multiple comparisons test was used. For all statistical tests,*P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001.
Techniques Used: Immunofluorescence, In Vitro, Control, Expressing, Ex Vivo, Methylation, Comparison
Figure Legend Snippet: a , Zoomed out image of Fig. 5a , localization of PDL1, F4/80, and CD11c near NINJA+ epithelium. 20x CellDIVE immunofluorescence image. Green = NINJA and Nur77, white = CD8b, red = F4/80.1, pink = PDL1, yellow = CD11c, orange = EpCAM. b , representative 20x CellDIVE immunofluorescence image of T cell-infiltrated NINJA+ islets. Green = NINJA, white = CD3, pink = PDL1, orange = insulin, blue = DAPI. n = 15, accross 2 experiments c , Violin plot of PDL1 transcript expression in various C57BL/6 mouse small intestine epithelial cell populations.
Techniques Used: Immunofluorescence, Expressing
Figure Legend Snippet: a ,Bubble plot of PDL1 methylation in various tissues and locations. b , bar graph depicting non-CpG CD274 methylation and downstream CpG promoter methylation.
Techniques Used: Methylation
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