mouse anti chicken cd3 mab (SouthernBiotech)
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SouthernBiotech
mouse anti chicken cd3 mab
Mouse Anti Chicken Cd3 Mab, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 93/100, based on 36 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+anti+chicken+iga+monoclonal+antibody/Mouse+Anti-Chicken+IgA-PE/pm39696681-52-7-11
Average 93 stars, based on 36 article reviews
Mouse Anti Chicken Cd3 Mab, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 93/100, based on 36 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+anti+chicken+iga+monoclonal+antibody/Mouse+Anti-Chicken+IgA-PE/pm39696681-52-7-11
Average 93 stars, based on 36 article reviews
mouse anti chicken cd3 mab - by Bioz Stars,
2026-10
93/100 stars
Images
1) Product Images from "Revealing novel and conservative CD8 + T-cell epitopes with MHC B2 restriction on ALV-J."
Article Title: Revealing novel and conservative CD8 + T-cell epitopes with MHC B2 restriction on ALV-J.
Journal: Veterinary research
doi: 10.1186/s13567-024-01426-3
Figure Legend Snippet: Figure 1 Detection of ALV-J shedding, ALV-J viremia, ALV-J antibody and T lymphocyte percentage of B2 haplotype chickens after ALV-J infection. Six chickens were randomly selected for sampling every 7 days post-infection (dpi). A ALV-J shedding was monitored via detecting the p27 expression levels in cloacal swabs. S/P value below 0.2 indicated negative ALV-J shedding. B ALV-J viremia was monitored via virus isolation. An S/P value above 0.2 indicated positive ALV-J viremia. C The ALV-J antibody level in the serum was monitored using the commercial ALV-J antibody test kit. An S/P value above 0.6 was considered ALV-J antibody positive. Five days before infection (dbi) and each week after infection, PBMCs derived from five chickens of infected and control groups were isolated to detect the T lymphocyte percentage, including the percentage of the CD4+CD3+T cell (D), the CD8α+CD3+T cell (E), and the CD3+CD4+CD8α+T cell (F). Each sample collected 1 × 105 cells for flow cytometric analysis. The one-way test was used for statistical comparison among A, B and C. And the unpaired Student t test was used for statistical comparison among D, E and F. * P < 0.05, ** P < 0.01.
Techniques Used: Infection, Sampling, Expressing, Virus, Isolation, Derivative Assay, Control, Comparison
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