anti mouse human tcf1 af488  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti mouse human tcf1 af488

    Anti Mouse Human Tcf1 Af488, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti mouse human tcf1 af488/product/Cell Signaling Technology Inc
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    Images

    1) Product Images from "IL-7-primed bystander CD8 tumor-infiltrating lymphocytes optimize the antitumor efficacy of T cell engager immunotherapy"

    Article Title: IL-7-primed bystander CD8 tumor-infiltrating lymphocytes optimize the antitumor efficacy of T cell engager immunotherapy

    Journal: Cell Reports Medicine

    doi: 10.1016/j.xcrm.2024.101567


    Figure Legend Snippet:

    Techniques Used: Purification, Recombinant, Formulation, Flow Cytometry, Amplification, Software, Staining

    anti human mouse tcf1 tcf7 af488  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc anti human mouse tcf1 tcf7 af488
    (A–D) Naive WT mice were treated with anti-CD137 (3H3, 10 μg) or IgG control mAbs. (A) Experimental design. (B–D) FACS plot and graphs showing Ki-67 expression by the indicated CD8 + T cell subsets along treatment. (E and F) The indicated CD45.1 CD8 + T cell subsets were injected i.v. into Cd137 −/− mice that were treated with anti-CD137 or IgG. (E) Experimental design. (F) FACS plot and graphs showing the frequency of CD45.1 + CD8 + T cells after 14 days. (G–K) WT mice were injected with anti-CD137 or IgG. The indicated splenic CD8 + T cell subsets were analyzed by scRNA-seq (n = 5–10 pooled mice/group). (G) Experimental design. (H and I) UMAP (H) and bar plots (I) showing CD8 + T cell cluster distribution. (J) Relative expression of Tnfrsf9 . (K) Clustered heatmap showing the indicated signature expression (1: Miller et al. ; 2: Siddiqui et al. ; 3: Utzschneider et al. ; 4: Giles et al. ). Data are scaled rowwise. (L) Clustered heatmap showing the 280 differentially expressed genes between Tex-like cells treated with anti-CD137 or Ig (log 2 FC > 0.25). (M–P) The indicated CD8 + T cell subsets isolated from WT mice treated with anti-CD137 were injected i.v. into Rag2 −/− Il2rg −/− mice treated with anti-CD137 or IgG. (M) Experimental design. (N) FACS plots and numbers of CD8 + T cells recovered after 7 days. (O) FACS plots and graphs showing PD1 and Tim3 expression and numbers. (P) Frequency of CD8 + T cells with a Tmem (CD44 hi PD1 − ), Tpex (PD1 + <t>TCF1</t> + Tim3 − ), or TermTex (PD1 + TCF1 − Tim3 + ) cell phenotype. Data are presented as mean ± SEM from at least 2 independent experiments. Each symbol represents an individual mouse. *p < 0.05; **p < 0.01, ***p < 0.001 (paired t test or ANOVA with Tukey’s post-test analysis).
    Anti Human Mouse Tcf1 Tcf7 Af488, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti human mouse tcf1 tcf7 af488/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti human mouse tcf1 tcf7 af488 - by Bioz Stars, 2024-09
    86/100 stars

    Images

    1) Product Images from "TCR-independent CD137 (4–1BB) signaling promotes CD8 + -exhausted T cell proliferation and terminal differentiation"

    Article Title: TCR-independent CD137 (4–1BB) signaling promotes CD8 + -exhausted T cell proliferation and terminal differentiation

    Journal: Immunity

    doi: 10.1016/j.immuni.2023.06.007

    (A–D) Naive WT mice were treated with anti-CD137 (3H3, 10 μg) or IgG control mAbs. (A) Experimental design. (B–D) FACS plot and graphs showing Ki-67 expression by the indicated CD8 + T cell subsets along treatment. (E and F) The indicated CD45.1 CD8 + T cell subsets were injected i.v. into Cd137 −/− mice that were treated with anti-CD137 or IgG. (E) Experimental design. (F) FACS plot and graphs showing the frequency of CD45.1 + CD8 + T cells after 14 days. (G–K) WT mice were injected with anti-CD137 or IgG. The indicated splenic CD8 + T cell subsets were analyzed by scRNA-seq (n = 5–10 pooled mice/group). (G) Experimental design. (H and I) UMAP (H) and bar plots (I) showing CD8 + T cell cluster distribution. (J) Relative expression of Tnfrsf9 . (K) Clustered heatmap showing the indicated signature expression (1: Miller et al. ; 2: Siddiqui et al. ; 3: Utzschneider et al. ; 4: Giles et al. ). Data are scaled rowwise. (L) Clustered heatmap showing the 280 differentially expressed genes between Tex-like cells treated with anti-CD137 or Ig (log 2 FC > 0.25). (M–P) The indicated CD8 + T cell subsets isolated from WT mice treated with anti-CD137 were injected i.v. into Rag2 −/− Il2rg −/− mice treated with anti-CD137 or IgG. (M) Experimental design. (N) FACS plots and numbers of CD8 + T cells recovered after 7 days. (O) FACS plots and graphs showing PD1 and Tim3 expression and numbers. (P) Frequency of CD8 + T cells with a Tmem (CD44 hi PD1 − ), Tpex (PD1 + TCF1 + Tim3 − ), or TermTex (PD1 + TCF1 − Tim3 + ) cell phenotype. Data are presented as mean ± SEM from at least 2 independent experiments. Each symbol represents an individual mouse. *p < 0.05; **p < 0.01, ***p < 0.001 (paired t test or ANOVA with Tukey’s post-test analysis).
    Figure Legend Snippet: (A–D) Naive WT mice were treated with anti-CD137 (3H3, 10 μg) or IgG control mAbs. (A) Experimental design. (B–D) FACS plot and graphs showing Ki-67 expression by the indicated CD8 + T cell subsets along treatment. (E and F) The indicated CD45.1 CD8 + T cell subsets were injected i.v. into Cd137 −/− mice that were treated with anti-CD137 or IgG. (E) Experimental design. (F) FACS plot and graphs showing the frequency of CD45.1 + CD8 + T cells after 14 days. (G–K) WT mice were injected with anti-CD137 or IgG. The indicated splenic CD8 + T cell subsets were analyzed by scRNA-seq (n = 5–10 pooled mice/group). (G) Experimental design. (H and I) UMAP (H) and bar plots (I) showing CD8 + T cell cluster distribution. (J) Relative expression of Tnfrsf9 . (K) Clustered heatmap showing the indicated signature expression (1: Miller et al. ; 2: Siddiqui et al. ; 3: Utzschneider et al. ; 4: Giles et al. ). Data are scaled rowwise. (L) Clustered heatmap showing the 280 differentially expressed genes between Tex-like cells treated with anti-CD137 or Ig (log 2 FC > 0.25). (M–P) The indicated CD8 + T cell subsets isolated from WT mice treated with anti-CD137 were injected i.v. into Rag2 −/− Il2rg −/− mice treated with anti-CD137 or IgG. (M) Experimental design. (N) FACS plots and numbers of CD8 + T cells recovered after 7 days. (O) FACS plots and graphs showing PD1 and Tim3 expression and numbers. (P) Frequency of CD8 + T cells with a Tmem (CD44 hi PD1 − ), Tpex (PD1 + TCF1 + Tim3 − ), or TermTex (PD1 + TCF1 − Tim3 + ) cell phenotype. Data are presented as mean ± SEM from at least 2 independent experiments. Each symbol represents an individual mouse. *p < 0.05; **p < 0.01, ***p < 0.001 (paired t test or ANOVA with Tukey’s post-test analysis).

    Techniques Used: Expressing, Injection, Isolation

    KEY RESOURCES TABLE
    Figure Legend Snippet: KEY RESOURCES TABLE

    Techniques Used: Purification, Recombinant, Lysis, Negative Control, Cell Isolation, Staining, Knock-Out, Isolation, Infection, RNA Sequencing Assay, Software, Expressing

    14456s anti human mouse tcf1 tcf7 af488  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc 14456s anti human mouse tcf1 tcf7 af488
    14456s Anti Human Mouse Tcf1 Tcf7 Af488, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/14456s anti human mouse tcf1 tcf7 af488/product/Cell Signaling Technology Inc
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    anti human tcf1 af488  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti human tcf1 af488
    Phenotypical profile of VACV/MPXV tetramer + CD8 + T cells in HBDs and mpox patients (A) Representative flow plots showing VACV/MPXV tetramer staining on CD8 + T cells (left) and frequencies (right). (B) Frequencies of naive and memory T cell subsets within tetramer + CD8 + T cells in HBDs and convalescent donors. (C) UMAP visualization of tetramer + CD8 + T cells from HBDs and convalescent donors, and expression of individual markers colored by marker expression levels. (D) Frequency of HLA-DR + CD38 + , Ki-67 + , Granzyme B + CD8 + T cells, and CXCR3 + expression in HBDs vs. convalescent donors. (E) Representative flow plots of transcription factors expression within VACV/MPXV + CD8 + T cells in HBDs vs. convalescent donors (left) and quantification (right). (F) Frequency of T-bet + CX3CR1 + terminally differentiated (effector) cells in HBDs vs. convalescent donors. (G) Spearman correlation of marker expression with time after symptom onset. (H and I) Frequency of MPXV-specific T SCM cells identified with tetramers (H) or AIM assay (I) after mild vs. moderate mpox. (J) Frequency of <t>TCF1</t> + cells and TCF1/T-bet ratio among tetramer + cells after mild vs. moderate mpox. In (A), (B), (D)–(F), and (H)–(J), Mann-Whitney test. In (G), Spearman rank correlation. See also <xref ref-type=Figure S4 . " width="250" height="auto" />
    Anti Human Tcf1 Af488, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti human tcf1 af488/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti human tcf1 af488 - by Bioz Stars, 2024-09
    86/100 stars

    Images

    1) Product Images from "Memory profiles distinguish cross-reactive and virus-specific T cell immunity to mpox"

    Article Title: Memory profiles distinguish cross-reactive and virus-specific T cell immunity to mpox

    Journal: Cell Host & Microbe

    doi: 10.1016/j.chom.2023.04.015

    Phenotypical profile of VACV/MPXV tetramer + CD8 + T cells in HBDs and mpox patients (A) Representative flow plots showing VACV/MPXV tetramer staining on CD8 + T cells (left) and frequencies (right). (B) Frequencies of naive and memory T cell subsets within tetramer + CD8 + T cells in HBDs and convalescent donors. (C) UMAP visualization of tetramer + CD8 + T cells from HBDs and convalescent donors, and expression of individual markers colored by marker expression levels. (D) Frequency of HLA-DR + CD38 + , Ki-67 + , Granzyme B + CD8 + T cells, and CXCR3 + expression in HBDs vs. convalescent donors. (E) Representative flow plots of transcription factors expression within VACV/MPXV + CD8 + T cells in HBDs vs. convalescent donors (left) and quantification (right). (F) Frequency of T-bet + CX3CR1 + terminally differentiated (effector) cells in HBDs vs. convalescent donors. (G) Spearman correlation of marker expression with time after symptom onset. (H and I) Frequency of MPXV-specific T SCM cells identified with tetramers (H) or AIM assay (I) after mild vs. moderate mpox. (J) Frequency of TCF1 + cells and TCF1/T-bet ratio among tetramer + cells after mild vs. moderate mpox. In (A), (B), (D)–(F), and (H)–(J), Mann-Whitney test. In (G), Spearman rank correlation. See also <xref ref-type=Figure S4 . " title="... after mild vs. moderate mpox. (J) Frequency of TCF1 + cells and TCF1/T-bet ratio among tetramer + ..." property="contentUrl" width="100%" height="100%"/>
    Figure Legend Snippet: Phenotypical profile of VACV/MPXV tetramer + CD8 + T cells in HBDs and mpox patients (A) Representative flow plots showing VACV/MPXV tetramer staining on CD8 + T cells (left) and frequencies (right). (B) Frequencies of naive and memory T cell subsets within tetramer + CD8 + T cells in HBDs and convalescent donors. (C) UMAP visualization of tetramer + CD8 + T cells from HBDs and convalescent donors, and expression of individual markers colored by marker expression levels. (D) Frequency of HLA-DR + CD38 + , Ki-67 + , Granzyme B + CD8 + T cells, and CXCR3 + expression in HBDs vs. convalescent donors. (E) Representative flow plots of transcription factors expression within VACV/MPXV + CD8 + T cells in HBDs vs. convalescent donors (left) and quantification (right). (F) Frequency of T-bet + CX3CR1 + terminally differentiated (effector) cells in HBDs vs. convalescent donors. (G) Spearman correlation of marker expression with time after symptom onset. (H and I) Frequency of MPXV-specific T SCM cells identified with tetramers (H) or AIM assay (I) after mild vs. moderate mpox. (J) Frequency of TCF1 + cells and TCF1/T-bet ratio among tetramer + cells after mild vs. moderate mpox. In (A), (B), (D)–(F), and (H)–(J), Mann-Whitney test. In (G), Spearman rank correlation. See also Figure S4 .

    Techniques Used: Staining, Expressing, Marker, MANN-WHITNEY


    Figure Legend Snippet:

    Techniques Used: Recombinant, Staining, Software

    anti mouse human tcf1 7 af488  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc anti mouse human tcf1 7 af488

    Anti Mouse Human Tcf1 7 Af488, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti mouse human tcf1 7 af488/product/Cell Signaling Technology Inc
    Average 93 stars, based on 1 article reviews
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    anti mouse human tcf1 7 af488 - by Bioz Stars, 2024-09
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    1) Product Images from "In situ maturation and tissue adaptation of type 2 innate lymphoid cell progenitors"

    Article Title: In situ maturation and tissue adaptation of type 2 innate lymphoid cell progenitors

    Journal: Immunity

    doi: 10.1016/j.immuni.2020.09.002


    Figure Legend Snippet:

    Techniques Used: Mouse Assay, Software

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    Cell Signaling Technology Inc anti mouse human tcf1 af488

    Anti Mouse Human Tcf1 Af488, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti mouse human tcf1 af488/product/Cell Signaling Technology Inc
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    Cell Signaling Technology Inc anti human mouse tcf1 tcf7 af488
    (A–D) Naive WT mice were treated with anti-CD137 (3H3, 10 μg) or IgG control mAbs. (A) Experimental design. (B–D) FACS plot and graphs showing Ki-67 expression by the indicated CD8 + T cell subsets along treatment. (E and F) The indicated CD45.1 CD8 + T cell subsets were injected i.v. into Cd137 −/− mice that were treated with anti-CD137 or IgG. (E) Experimental design. (F) FACS plot and graphs showing the frequency of CD45.1 + CD8 + T cells after 14 days. (G–K) WT mice were injected with anti-CD137 or IgG. The indicated splenic CD8 + T cell subsets were analyzed by scRNA-seq (n = 5–10 pooled mice/group). (G) Experimental design. (H and I) UMAP (H) and bar plots (I) showing CD8 + T cell cluster distribution. (J) Relative expression of Tnfrsf9 . (K) Clustered heatmap showing the indicated signature expression (1: Miller et al. ; 2: Siddiqui et al. ; 3: Utzschneider et al. ; 4: Giles et al. ). Data are scaled rowwise. (L) Clustered heatmap showing the 280 differentially expressed genes between Tex-like cells treated with anti-CD137 or Ig (log 2 FC > 0.25). (M–P) The indicated CD8 + T cell subsets isolated from WT mice treated with anti-CD137 were injected i.v. into Rag2 −/− Il2rg −/− mice treated with anti-CD137 or IgG. (M) Experimental design. (N) FACS plots and numbers of CD8 + T cells recovered after 7 days. (O) FACS plots and graphs showing PD1 and Tim3 expression and numbers. (P) Frequency of CD8 + T cells with a Tmem (CD44 hi PD1 − ), Tpex (PD1 + <t>TCF1</t> + Tim3 − ), or TermTex (PD1 + TCF1 − Tim3 + ) cell phenotype. Data are presented as mean ± SEM from at least 2 independent experiments. Each symbol represents an individual mouse. *p < 0.05; **p < 0.01, ***p < 0.001 (paired t test or ANOVA with Tukey’s post-test analysis).
    Anti Human Mouse Tcf1 Tcf7 Af488, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti human mouse tcf1 tcf7 af488/product/Cell Signaling Technology Inc
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    Cell Signaling Technology Inc 14456s anti human mouse tcf1 tcf7 af488
    (A–D) Naive WT mice were treated with anti-CD137 (3H3, 10 μg) or IgG control mAbs. (A) Experimental design. (B–D) FACS plot and graphs showing Ki-67 expression by the indicated CD8 + T cell subsets along treatment. (E and F) The indicated CD45.1 CD8 + T cell subsets were injected i.v. into Cd137 −/− mice that were treated with anti-CD137 or IgG. (E) Experimental design. (F) FACS plot and graphs showing the frequency of CD45.1 + CD8 + T cells after 14 days. (G–K) WT mice were injected with anti-CD137 or IgG. The indicated splenic CD8 + T cell subsets were analyzed by scRNA-seq (n = 5–10 pooled mice/group). (G) Experimental design. (H and I) UMAP (H) and bar plots (I) showing CD8 + T cell cluster distribution. (J) Relative expression of Tnfrsf9 . (K) Clustered heatmap showing the indicated signature expression (1: Miller et al. ; 2: Siddiqui et al. ; 3: Utzschneider et al. ; 4: Giles et al. ). Data are scaled rowwise. (L) Clustered heatmap showing the 280 differentially expressed genes between Tex-like cells treated with anti-CD137 or Ig (log 2 FC > 0.25). (M–P) The indicated CD8 + T cell subsets isolated from WT mice treated with anti-CD137 were injected i.v. into Rag2 −/− Il2rg −/− mice treated with anti-CD137 or IgG. (M) Experimental design. (N) FACS plots and numbers of CD8 + T cells recovered after 7 days. (O) FACS plots and graphs showing PD1 and Tim3 expression and numbers. (P) Frequency of CD8 + T cells with a Tmem (CD44 hi PD1 − ), Tpex (PD1 + <t>TCF1</t> + Tim3 − ), or TermTex (PD1 + TCF1 − Tim3 + ) cell phenotype. Data are presented as mean ± SEM from at least 2 independent experiments. Each symbol represents an individual mouse. *p < 0.05; **p < 0.01, ***p < 0.001 (paired t test or ANOVA with Tukey’s post-test analysis).
    14456s Anti Human Mouse Tcf1 Tcf7 Af488, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/14456s anti human mouse tcf1 tcf7 af488/product/Cell Signaling Technology Inc
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    Cell Signaling Technology Inc anti human tcf1 af488
    Phenotypical profile of VACV/MPXV tetramer + CD8 + T cells in HBDs and mpox patients (A) Representative flow plots showing VACV/MPXV tetramer staining on CD8 + T cells (left) and frequencies (right). (B) Frequencies of naive and memory T cell subsets within tetramer + CD8 + T cells in HBDs and convalescent donors. (C) UMAP visualization of tetramer + CD8 + T cells from HBDs and convalescent donors, and expression of individual markers colored by marker expression levels. (D) Frequency of HLA-DR + CD38 + , Ki-67 + , Granzyme B + CD8 + T cells, and CXCR3 + expression in HBDs vs. convalescent donors. (E) Representative flow plots of transcription factors expression within VACV/MPXV + CD8 + T cells in HBDs vs. convalescent donors (left) and quantification (right). (F) Frequency of T-bet + CX3CR1 + terminally differentiated (effector) cells in HBDs vs. convalescent donors. (G) Spearman correlation of marker expression with time after symptom onset. (H and I) Frequency of MPXV-specific T SCM cells identified with tetramers (H) or AIM assay (I) after mild vs. moderate mpox. (J) Frequency of <t>TCF1</t> + cells and TCF1/T-bet ratio among tetramer + cells after mild vs. moderate mpox. In (A), (B), (D)–(F), and (H)–(J), Mann-Whitney test. In (G), Spearman rank correlation. See also <xref ref-type=Figure S4 . " width="250" height="auto" />
    Anti Human Tcf1 Af488, supplied by Cell Signaling Technology Inc, 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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    Cell Signaling Technology Inc anti mouse human tcf1 7 af488

    Anti Mouse Human Tcf1 7 Af488, supplied by Cell Signaling Technology Inc, 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


    Journal: Cell Reports Medicine

    Article Title: IL-7-primed bystander CD8 tumor-infiltrating lymphocytes optimize the antitumor efficacy of T cell engager immunotherapy

    doi: 10.1016/j.xcrm.2024.101567

    Figure Lengend Snippet:

    Article Snippet: Anti-mouse/human TCF1 AF488 (clone: C63D9) , Cell Signaling , Cat# 6444S; RRID: AB_2797627.

    Techniques: Purification, Recombinant, Formulation, Flow Cytometry, Amplification, Software, Staining

    (A–D) Naive WT mice were treated with anti-CD137 (3H3, 10 μg) or IgG control mAbs. (A) Experimental design. (B–D) FACS plot and graphs showing Ki-67 expression by the indicated CD8 + T cell subsets along treatment. (E and F) The indicated CD45.1 CD8 + T cell subsets were injected i.v. into Cd137 −/− mice that were treated with anti-CD137 or IgG. (E) Experimental design. (F) FACS plot and graphs showing the frequency of CD45.1 + CD8 + T cells after 14 days. (G–K) WT mice were injected with anti-CD137 or IgG. The indicated splenic CD8 + T cell subsets were analyzed by scRNA-seq (n = 5–10 pooled mice/group). (G) Experimental design. (H and I) UMAP (H) and bar plots (I) showing CD8 + T cell cluster distribution. (J) Relative expression of Tnfrsf9 . (K) Clustered heatmap showing the indicated signature expression (1: Miller et al. ; 2: Siddiqui et al. ; 3: Utzschneider et al. ; 4: Giles et al. ). Data are scaled rowwise. (L) Clustered heatmap showing the 280 differentially expressed genes between Tex-like cells treated with anti-CD137 or Ig (log 2 FC > 0.25). (M–P) The indicated CD8 + T cell subsets isolated from WT mice treated with anti-CD137 were injected i.v. into Rag2 −/− Il2rg −/− mice treated with anti-CD137 or IgG. (M) Experimental design. (N) FACS plots and numbers of CD8 + T cells recovered after 7 days. (O) FACS plots and graphs showing PD1 and Tim3 expression and numbers. (P) Frequency of CD8 + T cells with a Tmem (CD44 hi PD1 − ), Tpex (PD1 + TCF1 + Tim3 − ), or TermTex (PD1 + TCF1 − Tim3 + ) cell phenotype. Data are presented as mean ± SEM from at least 2 independent experiments. Each symbol represents an individual mouse. *p < 0.05; **p < 0.01, ***p < 0.001 (paired t test or ANOVA with Tukey’s post-test analysis).

    Journal: Immunity

    Article Title: TCR-independent CD137 (4–1BB) signaling promotes CD8 + -exhausted T cell proliferation and terminal differentiation

    doi: 10.1016/j.immuni.2023.06.007

    Figure Lengend Snippet: (A–D) Naive WT mice were treated with anti-CD137 (3H3, 10 μg) or IgG control mAbs. (A) Experimental design. (B–D) FACS plot and graphs showing Ki-67 expression by the indicated CD8 + T cell subsets along treatment. (E and F) The indicated CD45.1 CD8 + T cell subsets were injected i.v. into Cd137 −/− mice that were treated with anti-CD137 or IgG. (E) Experimental design. (F) FACS plot and graphs showing the frequency of CD45.1 + CD8 + T cells after 14 days. (G–K) WT mice were injected with anti-CD137 or IgG. The indicated splenic CD8 + T cell subsets were analyzed by scRNA-seq (n = 5–10 pooled mice/group). (G) Experimental design. (H and I) UMAP (H) and bar plots (I) showing CD8 + T cell cluster distribution. (J) Relative expression of Tnfrsf9 . (K) Clustered heatmap showing the indicated signature expression (1: Miller et al. ; 2: Siddiqui et al. ; 3: Utzschneider et al. ; 4: Giles et al. ). Data are scaled rowwise. (L) Clustered heatmap showing the 280 differentially expressed genes between Tex-like cells treated with anti-CD137 or Ig (log 2 FC > 0.25). (M–P) The indicated CD8 + T cell subsets isolated from WT mice treated with anti-CD137 were injected i.v. into Rag2 −/− Il2rg −/− mice treated with anti-CD137 or IgG. (M) Experimental design. (N) FACS plots and numbers of CD8 + T cells recovered after 7 days. (O) FACS plots and graphs showing PD1 and Tim3 expression and numbers. (P) Frequency of CD8 + T cells with a Tmem (CD44 hi PD1 − ), Tpex (PD1 + TCF1 + Tim3 − ), or TermTex (PD1 + TCF1 − Tim3 + ) cell phenotype. Data are presented as mean ± SEM from at least 2 independent experiments. Each symbol represents an individual mouse. *p < 0.05; **p < 0.01, ***p < 0.001 (paired t test or ANOVA with Tukey’s post-test analysis).

    Article Snippet: Anti-human/mouse Tcf1/tcf7 AF488 [C63D9] , Cell Signaling Technology , Cat#: 6444S.

    Techniques: Expressing, Injection, Isolation

    KEY RESOURCES TABLE

    Journal: Immunity

    Article Title: TCR-independent CD137 (4–1BB) signaling promotes CD8 + -exhausted T cell proliferation and terminal differentiation

    doi: 10.1016/j.immuni.2023.06.007

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Anti-human/mouse Tcf1/tcf7 AF488 [C63D9] , Cell Signaling Technology , Cat#: 6444S.

    Techniques: Purification, Recombinant, Lysis, Negative Control, Cell Isolation, Staining, Knock-Out, Isolation, Infection, RNA Sequencing Assay, Software, Expressing

    Phenotypical profile of VACV/MPXV tetramer + CD8 + T cells in HBDs and mpox patients (A) Representative flow plots showing VACV/MPXV tetramer staining on CD8 + T cells (left) and frequencies (right). (B) Frequencies of naive and memory T cell subsets within tetramer + CD8 + T cells in HBDs and convalescent donors. (C) UMAP visualization of tetramer + CD8 + T cells from HBDs and convalescent donors, and expression of individual markers colored by marker expression levels. (D) Frequency of HLA-DR + CD38 + , Ki-67 + , Granzyme B + CD8 + T cells, and CXCR3 + expression in HBDs vs. convalescent donors. (E) Representative flow plots of transcription factors expression within VACV/MPXV + CD8 + T cells in HBDs vs. convalescent donors (left) and quantification (right). (F) Frequency of T-bet + CX3CR1 + terminally differentiated (effector) cells in HBDs vs. convalescent donors. (G) Spearman correlation of marker expression with time after symptom onset. (H and I) Frequency of MPXV-specific T SCM cells identified with tetramers (H) or AIM assay (I) after mild vs. moderate mpox. (J) Frequency of TCF1 + cells and TCF1/T-bet ratio among tetramer + cells after mild vs. moderate mpox. In (A), (B), (D)–(F), and (H)–(J), Mann-Whitney test. In (G), Spearman rank correlation. See also <xref ref-type=Figure S4 . " width="100%" height="100%">

    Journal: Cell Host & Microbe

    Article Title: Memory profiles distinguish cross-reactive and virus-specific T cell immunity to mpox

    doi: 10.1016/j.chom.2023.04.015

    Figure Lengend Snippet: Phenotypical profile of VACV/MPXV tetramer + CD8 + T cells in HBDs and mpox patients (A) Representative flow plots showing VACV/MPXV tetramer staining on CD8 + T cells (left) and frequencies (right). (B) Frequencies of naive and memory T cell subsets within tetramer + CD8 + T cells in HBDs and convalescent donors. (C) UMAP visualization of tetramer + CD8 + T cells from HBDs and convalescent donors, and expression of individual markers colored by marker expression levels. (D) Frequency of HLA-DR + CD38 + , Ki-67 + , Granzyme B + CD8 + T cells, and CXCR3 + expression in HBDs vs. convalescent donors. (E) Representative flow plots of transcription factors expression within VACV/MPXV + CD8 + T cells in HBDs vs. convalescent donors (left) and quantification (right). (F) Frequency of T-bet + CX3CR1 + terminally differentiated (effector) cells in HBDs vs. convalescent donors. (G) Spearman correlation of marker expression with time after symptom onset. (H and I) Frequency of MPXV-specific T SCM cells identified with tetramers (H) or AIM assay (I) after mild vs. moderate mpox. (J) Frequency of TCF1 + cells and TCF1/T-bet ratio among tetramer + cells after mild vs. moderate mpox. In (A), (B), (D)–(F), and (H)–(J), Mann-Whitney test. In (G), Spearman rank correlation. See also Figure S4 .

    Article Snippet: Anti-human TCF1 AF488 , CellSignaling , Cat# 6444S; RRID: AB_2199302.

    Techniques: Staining, Expressing, Marker, MANN-WHITNEY

    Journal: Cell Host & Microbe

    Article Title: Memory profiles distinguish cross-reactive and virus-specific T cell immunity to mpox

    doi: 10.1016/j.chom.2023.04.015

    Figure Lengend Snippet:

    Article Snippet: Anti-human TCF1 AF488 , CellSignaling , Cat# 6444S; RRID: AB_2199302.

    Techniques: Recombinant, Staining, Software

    Journal: Immunity

    Article Title: In situ maturation and tissue adaptation of type 2 innate lymphoid cell progenitors

    doi: 10.1016/j.immuni.2020.09.002

    Figure Lengend Snippet:

    Article Snippet: Anti-mouse/human TCF1/7 AF488 (Clone C63D9) , Cell Signalling , Cat # 6444S.

    Techniques: Mouse Assay, Software