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cd107a  (Bio-Rad)


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    Structured Review

    Bio-Rad cd107a
    Antigen-specific CD8 T-cell responses. Animals were immunized with eight vectors (red), GFP (gray), or nine vectors (blue) and boosted 28 days later. PBMCs purified on the indicated days were stimulated with peptide pools corresponding to the indicated gene products or the ubiquitinylated polyprotein (SW). The proportion of CD3 + CD8α + CD4 cells expressing IFNγ ( A–D ) or IFNγ and <t>CD107a</t> ( E–H ) 2 weeks post-prime ( A, D ), pre-boost ( B, E ), 7 days post-boost ( C, F ), and pre-challenge ( D, H ) was determined by flow cytometry. Each data point indicates a single animal, and bars show the mean of each group. Green fluorescent protein (GFP); interferon gamma (IFNγ); peripheral blood mononuclear cell (PBMC). * P ≤ 0.05, ** ≤ 0.01 .
    Cd107a, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cd107a/pmc13055240-4-0-13?v=Bio-Rad
    Average 94 stars, based on 20 article reviews
    cd107a - by Bioz Stars, 2026-06
    94/100 stars

    Images

    1) Product Images from "African swine fever virus genes vectored by simian adenoviruses do not protect against virulent genotype II virus challenge"

    Article Title: African swine fever virus genes vectored by simian adenoviruses do not protect against virulent genotype II virus challenge

    Journal: Microbiology Spectrum

    doi: 10.1128/spectrum.02328-25

    Antigen-specific CD8 T-cell responses. Animals were immunized with eight vectors (red), GFP (gray), or nine vectors (blue) and boosted 28 days later. PBMCs purified on the indicated days were stimulated with peptide pools corresponding to the indicated gene products or the ubiquitinylated polyprotein (SW). The proportion of CD3 + CD8α + CD4 cells expressing IFNγ ( A–D ) or IFNγ and CD107a ( E–H ) 2 weeks post-prime ( A, D ), pre-boost ( B, E ), 7 days post-boost ( C, F ), and pre-challenge ( D, H ) was determined by flow cytometry. Each data point indicates a single animal, and bars show the mean of each group. Green fluorescent protein (GFP); interferon gamma (IFNγ); peripheral blood mononuclear cell (PBMC). * P ≤ 0.05, ** ≤ 0.01 .
    Figure Legend Snippet: Antigen-specific CD8 T-cell responses. Animals were immunized with eight vectors (red), GFP (gray), or nine vectors (blue) and boosted 28 days later. PBMCs purified on the indicated days were stimulated with peptide pools corresponding to the indicated gene products or the ubiquitinylated polyprotein (SW). The proportion of CD3 + CD8α + CD4 cells expressing IFNγ ( A–D ) or IFNγ and CD107a ( E–H ) 2 weeks post-prime ( A, D ), pre-boost ( B, E ), 7 days post-boost ( C, F ), and pre-challenge ( D, H ) was determined by flow cytometry. Each data point indicates a single animal, and bars show the mean of each group. Green fluorescent protein (GFP); interferon gamma (IFNγ); peripheral blood mononuclear cell (PBMC). * P ≤ 0.05, ** ≤ 0.01 .

    Techniques Used: Purification, Expressing, Flow Cytometry

    Virus-specific CD8 T-cell responses. Animals were immunized with eight vectors (red), GFP (gray), or nine vectors (blue). Cells were purified from blood collected on the indicated days and stimulated with mock ( A, B ), OUR T1988/1 ( C, D ), or Georgia 2007/1 ( E, F ) inocula overnight and then treated with brefeldin A and anti-CD107a for 4 h. Populations of CD3 + CD8α + CD4 cells were then identified by flow cytometry, and the proportion of them expressing either IFNγ ( A, C, E ), IFNγ and CD107a ( B, D, F ) was determined. Each data point indicates a single animal, and bars show the mean of each group. Green fluorescent protein (GFP); interferon gamma (IFNγ). * P ≤ 0.05, ** ≤ 0.01 .
    Figure Legend Snippet: Virus-specific CD8 T-cell responses. Animals were immunized with eight vectors (red), GFP (gray), or nine vectors (blue). Cells were purified from blood collected on the indicated days and stimulated with mock ( A, B ), OUR T1988/1 ( C, D ), or Georgia 2007/1 ( E, F ) inocula overnight and then treated with brefeldin A and anti-CD107a for 4 h. Populations of CD3 + CD8α + CD4 cells were then identified by flow cytometry, and the proportion of them expressing either IFNγ ( A, C, E ), IFNγ and CD107a ( B, D, F ) was determined. Each data point indicates a single animal, and bars show the mean of each group. Green fluorescent protein (GFP); interferon gamma (IFNγ). * P ≤ 0.05, ** ≤ 0.01 .

    Techniques Used: Virus, Purification, Flow Cytometry, Expressing



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    Antigen-specific CD8 T-cell responses. Animals were immunized with eight vectors (red), GFP (gray), or nine vectors (blue) and boosted 28 days later. PBMCs purified on the indicated days were stimulated with peptide pools corresponding to the indicated gene products or the ubiquitinylated polyprotein (SW). The proportion of CD3 + CD8α + CD4 cells expressing IFNγ ( A–D ) or IFNγ and <t>CD107a</t> ( E–H ) 2 weeks post-prime ( A, D ), pre-boost ( B, E ), 7 days post-boost ( C, F ), and pre-challenge ( D, H ) was determined by flow cytometry. Each data point indicates a single animal, and bars show the mean of each group. Green fluorescent protein (GFP); interferon gamma (IFNγ); peripheral blood mononuclear cell (PBMC). * P ≤ 0.05, ** ≤ 0.01 .
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    Image Search Results


    Antigen-specific CD8 T-cell responses. Animals were immunized with eight vectors (red), GFP (gray), or nine vectors (blue) and boosted 28 days later. PBMCs purified on the indicated days were stimulated with peptide pools corresponding to the indicated gene products or the ubiquitinylated polyprotein (SW). The proportion of CD3 + CD8α + CD4 cells expressing IFNγ ( A–D ) or IFNγ and CD107a ( E–H ) 2 weeks post-prime ( A, D ), pre-boost ( B, E ), 7 days post-boost ( C, F ), and pre-challenge ( D, H ) was determined by flow cytometry. Each data point indicates a single animal, and bars show the mean of each group. Green fluorescent protein (GFP); interferon gamma (IFNγ); peripheral blood mononuclear cell (PBMC). * P ≤ 0.05, ** ≤ 0.01 .

    Journal: Microbiology Spectrum

    Article Title: African swine fever virus genes vectored by simian adenoviruses do not protect against virulent genotype II virus challenge

    doi: 10.1128/spectrum.02328-25

    Figure Lengend Snippet: Antigen-specific CD8 T-cell responses. Animals were immunized with eight vectors (red), GFP (gray), or nine vectors (blue) and boosted 28 days later. PBMCs purified on the indicated days were stimulated with peptide pools corresponding to the indicated gene products or the ubiquitinylated polyprotein (SW). The proportion of CD3 + CD8α + CD4 cells expressing IFNγ ( A–D ) or IFNγ and CD107a ( E–H ) 2 weeks post-prime ( A, D ), pre-boost ( B, E ), 7 days post-boost ( C, F ), and pre-challenge ( D, H ) was determined by flow cytometry. Each data point indicates a single animal, and bars show the mean of each group. Green fluorescent protein (GFP); interferon gamma (IFNγ); peripheral blood mononuclear cell (PBMC). * P ≤ 0.05, ** ≤ 0.01 .

    Article Snippet: CD107a , 4E9/11 , Mouse IgG1 , Alexa Fluor 647 , 1:100 , Bio-Rad Laboratories , MCA2315A647.

    Techniques: Purification, Expressing, Flow Cytometry

    Virus-specific CD8 T-cell responses. Animals were immunized with eight vectors (red), GFP (gray), or nine vectors (blue). Cells were purified from blood collected on the indicated days and stimulated with mock ( A, B ), OUR T1988/1 ( C, D ), or Georgia 2007/1 ( E, F ) inocula overnight and then treated with brefeldin A and anti-CD107a for 4 h. Populations of CD3 + CD8α + CD4 cells were then identified by flow cytometry, and the proportion of them expressing either IFNγ ( A, C, E ), IFNγ and CD107a ( B, D, F ) was determined. Each data point indicates a single animal, and bars show the mean of each group. Green fluorescent protein (GFP); interferon gamma (IFNγ). * P ≤ 0.05, ** ≤ 0.01 .

    Journal: Microbiology Spectrum

    Article Title: African swine fever virus genes vectored by simian adenoviruses do not protect against virulent genotype II virus challenge

    doi: 10.1128/spectrum.02328-25

    Figure Lengend Snippet: Virus-specific CD8 T-cell responses. Animals were immunized with eight vectors (red), GFP (gray), or nine vectors (blue). Cells were purified from blood collected on the indicated days and stimulated with mock ( A, B ), OUR T1988/1 ( C, D ), or Georgia 2007/1 ( E, F ) inocula overnight and then treated with brefeldin A and anti-CD107a for 4 h. Populations of CD3 + CD8α + CD4 cells were then identified by flow cytometry, and the proportion of them expressing either IFNγ ( A, C, E ), IFNγ and CD107a ( B, D, F ) was determined. Each data point indicates a single animal, and bars show the mean of each group. Green fluorescent protein (GFP); interferon gamma (IFNγ). * P ≤ 0.05, ** ≤ 0.01 .

    Article Snippet: CD107a , 4E9/11 , Mouse IgG1 , Alexa Fluor 647 , 1:100 , Bio-Rad Laboratories , MCA2315A647.

    Techniques: Virus, Purification, Flow Cytometry, Expressing