celltrace violet (ctv) proliferation kit Search Results


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Thermo Fisher celltrace violet cell proliferation kit
Celltrace Violet Cell Proliferation Kit, supplied by Thermo Fisher, 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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Thermo Fisher lipofectamine 3000 cat#l3000015
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Thermo Fisher celltrace violet kit
Celltrace Violet Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher celltrace violet™ (ctv) cell proliferation kit 422
Celltrace Violet™ (Ctv) Cell Proliferation Kit 422, supplied by Thermo Fisher, 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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Thermo Fisher celltracetm violet cell proliferation kit ctv
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Thermo Fisher cell trace violet ctv cell proliferation kit
Cell Trace Violet Ctv Cell Proliferation Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Thermo Fisher celltracetm violet (ctv) proliferation kit
( A ) <t>Proliferation</t> of <t>CTV-stained</t> CD4+ T-cell co-cultured with moDCs that had been pre-treated with dexamethasone (10 −7 M) for 24 h was suppressed compared to when co-cultured with untreated moDCs ( n = 16). The proportion of CD4+ T-cells that remained unproliferated (0 divisions) was higher when co-cultured with dexamethasone-treated moDCs, whereas CD4+ T-cells co-cultured with untreated DCs had undergone more divisions. ( B ) Treatment of DCs with neither UNC2025 (1 μM) ( n = 8) nor MIPS15692 10 μM ( n = 6) added to dexamethasone for 24 h had an additional effect on proliferation of co-cultured CD4+ T-cells. ( C ) Representative FACS histograms of CTV-stained CD4+ T cell proliferation when co-cultured with DCs that were untreated, treated with dexamethasone (10 −7 M), dexamethasone (10 −7 M) and UNC2025 (1 μM) for 24 h or in the absence of DCs. ( D ) Concentrations of pro-inflammatory cytokines ( n = 5) were reduced and anti-inflammatory cytokine TGF-β ( n = 13) was increased in dexamethasone-treated DC/T-cell co-cultures. ( E ) Proportions of DCs expressing CD80, CD86 and CD40 in DC/T-cell co-cultures were reduced with prior dexamethasone treatment but unchanged with addition of MIPS15692 ( n = 5). t -tests or one-way ANOVA were used to compare means between groups followed by Fisher’s Least Significant Difference for pre-selected conditions indicated by comparisons shown in each figure, with the exception of ( B ) where Kruskal–Wallis test was used to compare means between groups followed by Dunn’s post-hoc test for pre-selected conditions indicated by comparisons shown in each figure. “ns” indicates the result was not statistically significant.
Celltracetm Violet (Ctv) Proliferation Kit, supplied by Thermo Fisher, 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/result/celltracetm violet (ctv) proliferation kit/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
celltracetm violet (ctv) proliferation kit - by Bioz Stars, 2026-03
90/100 stars
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90
Thermo Fisher celltrace violet (ctv) labelling kit
( A ) <t>Proliferation</t> of <t>CTV-stained</t> CD4+ T-cell co-cultured with moDCs that had been pre-treated with dexamethasone (10 −7 M) for 24 h was suppressed compared to when co-cultured with untreated moDCs ( n = 16). The proportion of CD4+ T-cells that remained unproliferated (0 divisions) was higher when co-cultured with dexamethasone-treated moDCs, whereas CD4+ T-cells co-cultured with untreated DCs had undergone more divisions. ( B ) Treatment of DCs with neither UNC2025 (1 μM) ( n = 8) nor MIPS15692 10 μM ( n = 6) added to dexamethasone for 24 h had an additional effect on proliferation of co-cultured CD4+ T-cells. ( C ) Representative FACS histograms of CTV-stained CD4+ T cell proliferation when co-cultured with DCs that were untreated, treated with dexamethasone (10 −7 M), dexamethasone (10 −7 M) and UNC2025 (1 μM) for 24 h or in the absence of DCs. ( D ) Concentrations of pro-inflammatory cytokines ( n = 5) were reduced and anti-inflammatory cytokine TGF-β ( n = 13) was increased in dexamethasone-treated DC/T-cell co-cultures. ( E ) Proportions of DCs expressing CD80, CD86 and CD40 in DC/T-cell co-cultures were reduced with prior dexamethasone treatment but unchanged with addition of MIPS15692 ( n = 5). t -tests or one-way ANOVA were used to compare means between groups followed by Fisher’s Least Significant Difference for pre-selected conditions indicated by comparisons shown in each figure, with the exception of ( B ) where Kruskal–Wallis test was used to compare means between groups followed by Dunn’s post-hoc test for pre-selected conditions indicated by comparisons shown in each figure. “ns” indicates the result was not statistically significant.
Celltrace Violet (Ctv) Labelling Kit, supplied by Thermo Fisher, 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/result/celltrace violet (ctv) labelling kit/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
celltrace violet (ctv) labelling kit - by Bioz Stars, 2026-03
90/100 stars
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Image Search Results


( A ) Proliferation of CTV-stained CD4+ T-cell co-cultured with moDCs that had been pre-treated with dexamethasone (10 −7 M) for 24 h was suppressed compared to when co-cultured with untreated moDCs ( n = 16). The proportion of CD4+ T-cells that remained unproliferated (0 divisions) was higher when co-cultured with dexamethasone-treated moDCs, whereas CD4+ T-cells co-cultured with untreated DCs had undergone more divisions. ( B ) Treatment of DCs with neither UNC2025 (1 μM) ( n = 8) nor MIPS15692 10 μM ( n = 6) added to dexamethasone for 24 h had an additional effect on proliferation of co-cultured CD4+ T-cells. ( C ) Representative FACS histograms of CTV-stained CD4+ T cell proliferation when co-cultured with DCs that were untreated, treated with dexamethasone (10 −7 M), dexamethasone (10 −7 M) and UNC2025 (1 μM) for 24 h or in the absence of DCs. ( D ) Concentrations of pro-inflammatory cytokines ( n = 5) were reduced and anti-inflammatory cytokine TGF-β ( n = 13) was increased in dexamethasone-treated DC/T-cell co-cultures. ( E ) Proportions of DCs expressing CD80, CD86 and CD40 in DC/T-cell co-cultures were reduced with prior dexamethasone treatment but unchanged with addition of MIPS15692 ( n = 5). t -tests or one-way ANOVA were used to compare means between groups followed by Fisher’s Least Significant Difference for pre-selected conditions indicated by comparisons shown in each figure, with the exception of ( B ) where Kruskal–Wallis test was used to compare means between groups followed by Dunn’s post-hoc test for pre-selected conditions indicated by comparisons shown in each figure. “ns” indicates the result was not statistically significant.

Journal: International Journal of Molecular Sciences

Article Title: The Tolerogenic Influence of Dexamethasone on Dendritic Cells Is Accompanied by the Induction of Efferocytosis, Promoted by MERTK

doi: 10.3390/ijms242115903

Figure Lengend Snippet: ( A ) Proliferation of CTV-stained CD4+ T-cell co-cultured with moDCs that had been pre-treated with dexamethasone (10 −7 M) for 24 h was suppressed compared to when co-cultured with untreated moDCs ( n = 16). The proportion of CD4+ T-cells that remained unproliferated (0 divisions) was higher when co-cultured with dexamethasone-treated moDCs, whereas CD4+ T-cells co-cultured with untreated DCs had undergone more divisions. ( B ) Treatment of DCs with neither UNC2025 (1 μM) ( n = 8) nor MIPS15692 10 μM ( n = 6) added to dexamethasone for 24 h had an additional effect on proliferation of co-cultured CD4+ T-cells. ( C ) Representative FACS histograms of CTV-stained CD4+ T cell proliferation when co-cultured with DCs that were untreated, treated with dexamethasone (10 −7 M), dexamethasone (10 −7 M) and UNC2025 (1 μM) for 24 h or in the absence of DCs. ( D ) Concentrations of pro-inflammatory cytokines ( n = 5) were reduced and anti-inflammatory cytokine TGF-β ( n = 13) was increased in dexamethasone-treated DC/T-cell co-cultures. ( E ) Proportions of DCs expressing CD80, CD86 and CD40 in DC/T-cell co-cultures were reduced with prior dexamethasone treatment but unchanged with addition of MIPS15692 ( n = 5). t -tests or one-way ANOVA were used to compare means between groups followed by Fisher’s Least Significant Difference for pre-selected conditions indicated by comparisons shown in each figure, with the exception of ( B ) where Kruskal–Wallis test was used to compare means between groups followed by Dunn’s post-hoc test for pre-selected conditions indicated by comparisons shown in each figure. “ns” indicates the result was not statistically significant.

Article Snippet: CellTraceTM Violet (CTV) proliferation kit (ThermoFisher Scientific, Waltham, MA, USA) was used to assess proliferation of magnetically isolated CD4+ T cells according to manufacturer protocol.

Techniques: Staining, Cell Culture, Expressing