cd3positive enrichment kit Search Results


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Miltenyi Biotec cd3 enrichment assay kit
Cd3 Enrichment Assay Kit, supplied by Miltenyi Biotec, 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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STEMCELL Technologies Inc cd3positive enrichment kit
Cd3positive Enrichment Kit, 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
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STEMCELL Technologies Inc mouse cd3 t-cell enrichment kit
a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating <t>CD3</t> + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.
Mouse Cd3 T Cell Enrichment Kit, 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
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STEMCELL Technologies Inc cd3 positive selection kit ii
a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating <t>CD3</t> + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.
Cd3 Positive Selection Kit Ii, 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
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STEMCELL Technologies Inc cd3 human t-cell enrichment kit
a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating <t>CD3</t> + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.
Cd3 Human T Cell Enrichment Kit, 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
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STEMCELL Technologies Inc cd3 + t cell enrichment kit easysep human t cell enrichment
a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating <t>CD3</t> + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.
Cd3 + T Cell Enrichment Kit Easysep Human T Cell Enrichment, 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
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Miltenyi Biotec cd3 cd28 activation beads
a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating <t>CD3</t> + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.
Cd3 Cd28 Activation Beads, supplied by Miltenyi Biotec, 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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STEMCELL Technologies Inc positive cd3 cell selection kit ii
a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating <t>CD3</t> + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.
Positive Cd3 Cell Selection Kit Ii, 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
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Miltenyi Biotec lin conjugated immunomagnetic negative selection kit
a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating <t>CD3</t> + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.
Lin Conjugated Immunomagnetic Negative Selection Kit, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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STEMCELL Technologies Inc spinsep mouse cd3 + t cell enrichment kit
a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating <t>CD3</t> + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.
Spinsep Mouse Cd3 + T Cell Enrichment Kit, 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
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R&D Systems mouse cd3 t cell column enrichment kit
a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating <t>CD3</t> + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.
Mouse Cd3 T Cell Column Enrichment Kit, supplied by R&D Systems, 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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STEMCELL Technologies Inc cd3 t cell isolation kit
a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating <t>CD3</t> + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.
Cd3 T Cell Isolation Kit, 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
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Image Search Results


a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating CD3 + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.

Journal: Nature Communications

Article Title: Cationic crosslinked carbon dots-adjuvanted intranasal vaccine induces protective immunity against Omicron-included SARS-CoV-2 variants

doi: 10.1038/s41467-023-38066-8

Figure Lengend Snippet: a The percentages of Tfh (CD4 + CXCR5 + PD-1 + ) and RBD-specific GCB (B220 + GL7 + CD95 + RBD + ) cells in the CLN were analyzed with FCM at 28 days after the last immunization. b , c Lung CD8 + and CD4 + T cells were evaluated for IFN-γ generation by FCM upon restimulation with RBD peptide pools or irrelevant antigens. b Representative FCM plots (left) and quantification (right) of IFN-γ-expressing lung CD8 + T cells. d The proportion of antigen-experienced (CD44 + ) CD4 + and CD8 + T cells expressing CD69 and CD103 in lung tissues. e The percentage of CD103 + DCs coexpressing CD86 and MHC II in the lungs. f Upper left: t-SNE maps were created by concentrating CD3 + T cells from the BAL fluid of the vaccinated mice. Analysis was carried out with default FlowJo V.10 software. Upper right and bottom: heatmap projections of CD4, CD8, CD44, CD69, and CD103 expression on t-SNE maps from three independent mice ( n = 3). Red and black hashed circles are indicators of antigen-experienced CD4 + and CD8 + T RM cells in the BAL fluid, respectively. g Absolute numbers of CD8 + T cells producing IFN-γ (left) and TNF-α (right) in the BAL after ex vivo restimulation with RBD peptide pools or irrelevant antigen at 4 weeks after the last immunization. h Quantification of the percentages (left) and the numbers (right) of MHC II + AM in the BAL fluid. Data were displayed with floating bars in ( a – e , g , and h ). The middle line indicates the median and the box shows the data range. Data were presented as mean values ± SEM. n = 4–6 mice in each group in ( a – e , g , and h ). P values in a , d , e , h were calculated with One-way ANOVA followed by Dunnett’s multiple comparisons tests. P values in b , c , and g were calculated with two-way ANOVA followed by Tukey’s multiple comparisons tests. Source data are provided as a Source Data file.

Article Snippet: T cells in untreated, female, 6–8 weeks BALB/c mouse spleen were obtained by a mouse CD3 T-cell enrichment kit (Stemcell).

Techniques: Expressing, Software, Ex Vivo