fitc antimouse-cd3 antibody Search Results


94
Cell Signaling Technology Inc antimouse cd3
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
Antimouse Cd3, supplied by Cell Signaling Technology Inc, 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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Average 94 stars, based on 1 article reviews
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90
Becton Dickinson fitc-conjugated rat antimouse-cd3
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
Fitc Conjugated Rat Antimouse Cd3, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+antimouse-cd3+antibody/pm19016769-73-43-46?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
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93
Bio-Rad 145 2c11
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
145 2c11, supplied by Bio-Rad, 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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94
Bio-Rad fluorescein isothiocyanate fitc conjugated rat antimouse cd3
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
Fluorescein Isothiocyanate Fitc Conjugated Rat Antimouse Cd3, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+antimouse-cd3+antibody/pm31818168-57-12-18?v=Bio-Rad
Average 94 stars, based on 1 article reviews
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90
Becton Dickinson phycoerythrin (pe)-cy5.5-labeled antimouse cd3
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
Phycoerythrin (Pe) Cy5.5 Labeled Antimouse Cd3, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+antimouse-cd3+antibody/pmc04002679-44-2-17?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
phycoerythrin (pe)-cy5.5-labeled antimouse cd3 - by Bioz Stars, 2026-08
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90
STEMCELL Technologies Inc antimouse cd3 antibody stemcell 60015fi
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
Antimouse Cd3 Antibody Stemcell 60015fi, supplied by STEMCELL Technologies Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+antimouse-cd3+antibody/pm35477832-80-31-34?v=STEMCELL+Technologies+Inc
Average 90 stars, based on 1 article reviews
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99
NSJ Bioreagents cd3 epsilon antibody
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
Cd3 Epsilon Antibody, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+antimouse-cd3+antibody/custom%40v8271%40pm39007530__nl4c02113_si_001?v=NSJ+Bioreagents
Average 99 stars, based on 1 article reviews
cd3 epsilon antibody - by Bioz Stars, 2026-08
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99
Biotium cd3e, mouse(145-2c11)
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
Cd3e, Mouse(145 2c11), supplied by Biotium, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
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99
NSJ Bioreagents cd4 antibody
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
Cd4 Antibody, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fitc+antimouse-cd3+antibody/custom%40v8352%4034949694?v=NSJ+Bioreagents
Average 99 stars, based on 1 article reviews
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NSJ Bioreagents nk1.1 antibody / cd161c
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
Nk1.1 Antibody / Cd161c, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
nk1.1 antibody / cd161c - by Bioz Stars, 2026-08
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99
NSJ Bioreagents cd11b antibody / mac-1
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
Cd11b Antibody / Mac 1, supplied by NSJ Bioreagents, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Becton Dickinson pe antimouse mac-3
Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive <t>CD3+</t> + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of <t>CD3-positive</t> T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm
Pe Antimouse Mac 3, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
pe antimouse mac-3 - by Bioz Stars, 2026-08
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Image Search Results


Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive CD3+ + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of CD3-positive T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm

Journal: BMC immunology

Article Title: IL-6 and PD-1 antibody blockade combination therapy regulate inflammation and T lymphocyte apoptosis in murine model of sepsis.

doi: 10.1186/s12865-024-00679-z

Figure Lengend Snippet: Fig. 7 Immunofluorescence staining of cleaved-caspase-3⁺ and CD3⁺ in the spleen samples from each group of mice. A Double immunofluorescence staining in the sham, CLP, anti-IL-6, anti-PD-1, and anti-IL-6/PD-1 mice groups were used to analyze the expression levels of cleaved-caspase-3⁺ and CD3⁺ in the spleen cells of mice. Cleaved-caspase-3⁺ cells and CD3⁺ cells showed red and green fluorescence, respectively. The nuclei were stained using DAPI (blue fluorescence). The final panel shows the merged double-positive CD3+ + cleaved-caspase-3⁺ + DAPI-stained cells. B Quantification of CD3-positive T-cell count per field. C Quantification of cleaved caspase-3-positive apoptotic cell count per field. Data are expressed as median and interquartile range; *p < 0.05, **p < 0.005, ***p < 0.001, as determined by one-way ANOVA with post-hoc Tukey’s multiple comparison test. Scale bar: 50 μm

Article Snippet: Immunohistochemical staining of lymphocyte apoptosis in the 3-μm paraffin-embedded tissue sections of the spleen was conducted using antimouse CD3 + (Lymphocyte; CD3 [17A2] Rat mAb [FITC Conjugate]; Cell Signaling Technology; 86603), cleaved caspase-3 (Cleaved Caspase-3 [Asp175] [5A1E] Rabbit mAb; Cell Signaling Technology; 9664), and DAPI.

Techniques: Immunofluorescence, Staining, Double Immunofluorescence Staining, Expressing, Fluorescence, Cell Counting, Comparison