t lymphocytes Search Results


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E0089hu, supplied by Shanghai Korain Biotech Co Ltd, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio antihuman cd19 antibody
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Bio-Rad mouse anti rabbit t lymphocytes
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Boster Bio interleukin 17
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Boster Bio granulysin
Expression of cytolytic molecules in plasma of HCs ( n = 16) and AS patients ( n = 16). The plasma levels of granzyme A (A), granzyme B (B) and <t>granulysin</t> (C) were determined by enzyme‐linked immunosorbent assay. Pearson correlation analysis was performed between granzyme A (D), granzyme B (E), granulysin (F) and disease activity (BASDAI). Horizontal lines and error bars show the mean ± SEM. ** p < 0.01; *** p < 0.001; ns = not significant
Granulysin, supplied by Boster Bio, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio cd8
Expression of cytolytic molecules in plasma of HCs ( n = 16) and AS patients ( n = 16). The plasma levels of granzyme A (A), granzyme B (B) and <t>granulysin</t> (C) were determined by enzyme‐linked immunosorbent assay. Pearson correlation analysis was performed between granzyme A (D), granzyme B (E), granulysin (F) and disease activity (BASDAI). Horizontal lines and error bars show the mean ± SEM. ** p < 0.01; *** p < 0.001; ns = not significant
Cd8, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio anti bodies
Expression of cytolytic molecules in plasma of HCs ( n = 16) and AS patients ( n = 16). The plasma levels of granzyme A (A), granzyme B (B) and <t>granulysin</t> (C) were determined by enzyme‐linked immunosorbent assay. Pearson correlation analysis was performed between granzyme A (D), granzyme B (E), granulysin (F) and disease activity (BASDAI). Horizontal lines and error bars show the mean ± SEM. ** p < 0.01; *** p < 0.001; ns = not significant
Anti Bodies, supplied by Boster Bio, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ProSci Incorporated monoclonal antibody mab
Expression of cytolytic molecules in plasma of HCs ( n = 16) and AS patients ( n = 16). The plasma levels of granzyme A (A), granzyme B (B) and <t>granulysin</t> (C) were determined by enzyme‐linked immunosorbent assay. Pearson correlation analysis was performed between granzyme A (D), granzyme B (E), granulysin (F) and disease activity (BASDAI). Horizontal lines and error bars show the mean ± SEM. ** p < 0.01; *** p < 0.001; ns = not significant
Monoclonal Antibody Mab, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio il 17
Expression of cytolytic molecules in plasma of HCs ( n = 16) and AS patients ( n = 16). The plasma levels of granzyme A (A), granzyme B (B) and <t>granulysin</t> (C) were determined by enzyme‐linked immunosorbent assay. Pearson correlation analysis was performed between granzyme A (D), granzyme B (E), granulysin (F) and disease activity (BASDAI). Horizontal lines and error bars show the mean ± SEM. ** p < 0.01; *** p < 0.001; ns = not significant
Il 17, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Boster Bio anti-cd80
Expression of cytolytic molecules in plasma of HCs ( n = 16) and AS patients ( n = 16). The plasma levels of granzyme A (A), granzyme B (B) and <t>granulysin</t> (C) were determined by enzyme‐linked immunosorbent assay. Pearson correlation analysis was performed between granzyme A (D), granzyme B (E), granulysin (F) and disease activity (BASDAI). Horizontal lines and error bars show the mean ± SEM. ** p < 0.01; *** p < 0.001; ns = not significant
Anti Cd80, supplied by Boster Bio, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Proteintech cd19 antibody
CD39 inhibitor combined with PD-1 blockade improved therapeutic efficacy by promoting CXCL13 release and B cell activation . ( A ) Enzyme-linked immunosorbent assay (ELISA) was used to detect the content of CXCL13 in the serum samples of isotype, αPD-1, CD39i, and combined treatment groups of mice. ( B ) The content of CXCL13 in murine tumors was detected using ELISA. ( C ) Flow cytometry allowed detection of the proportion of CXCR5 + B cells in murine tumors. ( D - E ) Flow cytometry ( D ) and dot plots ( E ) showed the proportion of activated B cell infiltration in murine tumors. ( F ) The dot plot displayed the proportion of GCB cells in tumor B220 + B cells. ( G , H ) Dot plots showed the proportion of dark zone (DZ) ( G ) and light zone (LZ) ( H ) in GCB cells in mouse tumors. ( I , J ) Representative histograms ( I ) and summarized Mean Fluorescence Intensity (MFI) diagram ( J ) showed the expression of BCL6 in GCB cells. ( K ) The dot plot showed the proportion of plasma cells among <t>CD19</t> + B cells of mouse tumors. ( L ) The dot plot displayed the proportion of memory B cells in mouse tumor B220 + B cells. The values were obtained using the Kruskal–Wallis test. * , P < 0.05; ** , P < 0.01; ***; P < 0.001; ns , not significant . Abbreviations: GCB, geminal center B cells; DZ, dark zone; LZ, light zone
Cd19 Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Expression of cytolytic molecules in plasma of HCs ( n = 16) and AS patients ( n = 16). The plasma levels of granzyme A (A), granzyme B (B) and granulysin (C) were determined by enzyme‐linked immunosorbent assay. Pearson correlation analysis was performed between granzyme A (D), granzyme B (E), granulysin (F) and disease activity (BASDAI). Horizontal lines and error bars show the mean ± SEM. ** p < 0.01; *** p < 0.001; ns = not significant

Journal: Journal of Cellular and Molecular Medicine

Article Title: Single‐cell RNA‐seq reveals altered NK cell subsets and reduced levels of cytotoxic molecules in patients with ankylosing spondylitis

doi: 10.1111/jcmm.17159

Figure Lengend Snippet: Expression of cytolytic molecules in plasma of HCs ( n = 16) and AS patients ( n = 16). The plasma levels of granzyme A (A), granzyme B (B) and granulysin (C) were determined by enzyme‐linked immunosorbent assay. Pearson correlation analysis was performed between granzyme A (D), granzyme B (E), granulysin (F) and disease activity (BASDAI). Horizontal lines and error bars show the mean ± SEM. ** p < 0.01; *** p < 0.001; ns = not significant

Article Snippet: Plasma levels of cytotoxic granules, including GZMA, GZMB and granulysin, were quantified using ELISA kits (#EK1162, #EK1114 and # EK1280, BOSTER Biological Technology).

Techniques: Expressing, Clinical Proteomics, Enzyme-linked Immunosorbent Assay, Activity Assay

CD39 inhibitor combined with PD-1 blockade improved therapeutic efficacy by promoting CXCL13 release and B cell activation . ( A ) Enzyme-linked immunosorbent assay (ELISA) was used to detect the content of CXCL13 in the serum samples of isotype, αPD-1, CD39i, and combined treatment groups of mice. ( B ) The content of CXCL13 in murine tumors was detected using ELISA. ( C ) Flow cytometry allowed detection of the proportion of CXCR5 + B cells in murine tumors. ( D - E ) Flow cytometry ( D ) and dot plots ( E ) showed the proportion of activated B cell infiltration in murine tumors. ( F ) The dot plot displayed the proportion of GCB cells in tumor B220 + B cells. ( G , H ) Dot plots showed the proportion of dark zone (DZ) ( G ) and light zone (LZ) ( H ) in GCB cells in mouse tumors. ( I , J ) Representative histograms ( I ) and summarized Mean Fluorescence Intensity (MFI) diagram ( J ) showed the expression of BCL6 in GCB cells. ( K ) The dot plot showed the proportion of plasma cells among CD19 + B cells of mouse tumors. ( L ) The dot plot displayed the proportion of memory B cells in mouse tumor B220 + B cells. The values were obtained using the Kruskal–Wallis test. * , P < 0.05; ** , P < 0.01; ***; P < 0.001; ns , not significant . Abbreviations: GCB, geminal center B cells; DZ, dark zone; LZ, light zone

Journal: Journal of Nanobiotechnology

Article Title: Targeting CD39 boosts PD-1 blockade antitumor therapeutic efficacy via strengthening CD8 + TILs function and recruiting B cells in cervical cancer

doi: 10.1186/s12951-025-03500-0

Figure Lengend Snippet: CD39 inhibitor combined with PD-1 blockade improved therapeutic efficacy by promoting CXCL13 release and B cell activation . ( A ) Enzyme-linked immunosorbent assay (ELISA) was used to detect the content of CXCL13 in the serum samples of isotype, αPD-1, CD39i, and combined treatment groups of mice. ( B ) The content of CXCL13 in murine tumors was detected using ELISA. ( C ) Flow cytometry allowed detection of the proportion of CXCR5 + B cells in murine tumors. ( D - E ) Flow cytometry ( D ) and dot plots ( E ) showed the proportion of activated B cell infiltration in murine tumors. ( F ) The dot plot displayed the proportion of GCB cells in tumor B220 + B cells. ( G , H ) Dot plots showed the proportion of dark zone (DZ) ( G ) and light zone (LZ) ( H ) in GCB cells in mouse tumors. ( I , J ) Representative histograms ( I ) and summarized Mean Fluorescence Intensity (MFI) diagram ( J ) showed the expression of BCL6 in GCB cells. ( K ) The dot plot showed the proportion of plasma cells among CD19 + B cells of mouse tumors. ( L ) The dot plot displayed the proportion of memory B cells in mouse tumor B220 + B cells. The values were obtained using the Kruskal–Wallis test. * , P < 0.05; ** , P < 0.01; ***; P < 0.001; ns , not significant . Abbreviations: GCB, geminal center B cells; DZ, dark zone; LZ, light zone

Article Snippet: The sections were stained with a CD19 antibody (27949-1-AP; Proteintech; 1:500), Ki67 antibody(ab16667;Abcam;1:200), TUNEL antibody(G1507; Servicebio; 1:200) followed by a secondary antibody (GB23303; Servicebio; 1:200).

Techniques: Drug discovery, Activation Assay, Enzyme-linked Immunosorbent Assay, Flow Cytometry, Fluorescence, Expressing, Clinical Proteomics