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pe anti mouse cd366 tim 3  (Miltenyi Biotec)


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    Miltenyi Biotec pe anti mouse cd366 tim 3
    Pe Anti Mouse Cd366 Tim 3, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 92/100, based on 20 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pe+anti+mouse+cd366+tim+3/CD366+(TIM-3)+Antibody%2C+anti-mouse%2C+REAfinity/pmc13006431-62-0-7
    Average 92 stars, based on 20 article reviews
    pe anti mouse cd366 tim 3 - by Bioz Stars, 2026-10
    92/100 stars

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    other:

    Article Title: Valrubicin-loaded immunoliposomes targeting antigens on immunosuppressive cells to circumvent resistance to cancer immunotherapy
    Article Snippet: PE anti-Mouse CD366 (TIM-3) (Clone REA602) , Miltenyi Biotec , Cat# 130-118-691; RRID: AB_2733707.



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    pe anti mouse cd366 tim 3  (Miltenyi Biotec)
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    Pe Anti Mouse Cd366 Tim 3, supplied by Miltenyi Biotec, 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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    pe dazzle tm 594 anti mouse cd366 tim 3 antibody  (Cell Signaling Technology Inc)
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    (A and B) Tumor growth kinetics (A) and mass (B) of WT or miR-155 TKO mice challenged with MC38 cells and administered ICI or PBS 4, 7, and 10 d.p.i. (red arrows). Data were pooled from two replicate experiments; n = 11–22; robust regression and outlier removal (ROUT) outlier test (Q = 1%). (C–P) Representative frequency and number of CD8 + T cells/g of tumor (C and D) and intratumoral frequency of Gzmb + (E and G), IFNγ + (F and H), PD-1 + (I and K), <t>Tim-3</t> + (J and L), Tscm CD44 − CD62L + (M and N), CM CD44 + CD62L + (M and O), and eff CD44 + CD62L − (M and P) CD8 + T cells; n = 7–10. One-way ANOVA with multiple comparisons of means of each group; * p > 0.05, ** p > 0.01, *** p > 0.001, **** p > 0.0001. Bars represent mean; error bars represent SEM. See also .
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    (A and B) Tumor growth kinetics (A) and mass (B) of WT or miR-155 TKO mice challenged with MC38 cells and administered ICI or PBS 4, 7, and 10 d.p.i. (red arrows). Data were pooled from two replicate experiments; n = 11–22; robust regression and outlier removal (ROUT) outlier test (Q = 1%). (C–P) Representative frequency and number of CD8 + T cells/g of tumor (C and D) and intratumoral frequency of Gzmb + (E and G), IFNγ + (F and H), PD-1 + (I and K), <t>Tim-3</t> + (J and L), Tscm CD44 − CD62L + (M and N), CM CD44 + CD62L + (M and O), and eff CD44 + CD62L − (M and P) CD8 + T cells; n = 7–10. One-way ANOVA with multiple comparisons of means of each group; * p > 0.05, ** p > 0.01, *** p > 0.001, **** p > 0.0001. Bars represent mean; error bars represent SEM. See also .
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    (A and B) Tumor growth kinetics (A) and mass (B) of WT or miR-155 TKO mice challenged with MC38 cells and administered ICI or PBS 4, 7, and 10 d.p.i. (red arrows). Data were pooled from two replicate experiments; n = 11–22; robust regression and outlier removal (ROUT) outlier test (Q = 1%). (C–P) Representative frequency and number of CD8 + T cells/g of tumor (C and D) and intratumoral frequency of Gzmb + (E and G), IFNγ + (F and H), PD-1 + (I and K), <t>Tim-3</t> + (J and L), Tscm CD44 − CD62L + (M and N), CM CD44 + CD62L + (M and O), and eff CD44 + CD62L − (M and P) CD8 + T cells; n = 7–10. One-way ANOVA with multiple comparisons of means of each group; * p > 0.05, ** p > 0.01, *** p > 0.001, **** p > 0.0001. Bars represent mean; error bars represent SEM. See also .
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    (A and B) Tumor growth kinetics (A) and mass (B) of WT or miR-155 TKO mice challenged with MC38 cells and administered ICI or PBS 4, 7, and 10 d.p.i. (red arrows). Data were pooled from two replicate experiments; n = 11–22; robust regression and outlier removal (ROUT) outlier test (Q = 1%). (C–P) Representative frequency and number of CD8 + T cells/g of tumor (C and D) and intratumoral frequency of Gzmb + (E and G), IFNγ + (F and H), PD-1 + (I and K), <t>Tim-3</t> + (J and L), Tscm CD44 − CD62L + (M and N), CM CD44 + CD62L + (M and O), and eff CD44 + CD62L − (M and P) CD8 + T cells; n = 7–10. One-way ANOVA with multiple comparisons of means of each group; * p > 0.05, ** p > 0.01, *** p > 0.001, **** p > 0.0001. Bars represent mean; error bars represent SEM. See also .
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    (A and B) Tumor growth kinetics (A) and mass (B) of WT or miR-155 TKO mice challenged with MC38 cells and administered ICI or PBS 4, 7, and 10 d.p.i. (red arrows). Data were pooled from two replicate experiments; n = 11–22; robust regression and outlier removal (ROUT) outlier test (Q = 1%). (C–P) Representative frequency and number of CD8 + T cells/g of tumor (C and D) and intratumoral frequency of Gzmb + (E and G), IFNγ + (F and H), PD-1 + (I and K), <t>Tim-3</t> + (J and L), Tscm CD44 − CD62L + (M and N), CM CD44 + CD62L + (M and O), and eff CD44 + CD62L − (M and P) CD8 + T cells; n = 7–10. One-way ANOVA with multiple comparisons of means of each group; * p > 0.05, ** p > 0.01, *** p > 0.001, **** p > 0.0001. Bars represent mean; error bars represent SEM. See also .
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    (A and B) Tumor growth kinetics (A) and mass (B) of WT or miR-155 TKO mice challenged with MC38 cells and administered ICI or PBS 4, 7, and 10 d.p.i. (red arrows). Data were pooled from two replicate experiments; n = 11–22; robust regression and outlier removal (ROUT) outlier test (Q = 1%). (C–P) Representative frequency and number of CD8 + T cells/g of tumor (C and D) and intratumoral frequency of Gzmb + (E and G), IFNγ + (F and H), PD-1 + (I and K), <t>Tim-3</t> + (J and L), Tscm CD44 − CD62L + (M and N), CM CD44 + CD62L + (M and O), and eff CD44 + CD62L − (M and P) CD8 + T cells; n = 7–10. One-way ANOVA with multiple comparisons of means of each group; * p > 0.05, ** p > 0.01, *** p > 0.001, **** p > 0.0001. Bars represent mean; error bars represent SEM. See also .
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    (A and B) Tumor growth kinetics (A) and mass (B) of WT or miR-155 TKO mice challenged with MC38 cells and administered ICI or PBS 4, 7, and 10 d.p.i. (red arrows). Data were pooled from two replicate experiments; n = 11–22; robust regression and outlier removal (ROUT) outlier test (Q = 1%). (C–P) Representative frequency and number of CD8 + T cells/g of tumor (C and D) and intratumoral frequency of Gzmb + (E and G), IFNγ + (F and H), PD-1 + (I and K), <t>Tim-3</t> + (J and L), Tscm CD44 − CD62L + (M and N), CM CD44 + CD62L + (M and O), and eff CD44 + CD62L − (M and P) CD8 + T cells; n = 7–10. One-way ANOVA with multiple comparisons of means of each group; * p > 0.05, ** p > 0.01, *** p > 0.001, **** p > 0.0001. Bars represent mean; error bars represent SEM. See also .
    Tim 3 Pe, supplied by Miltenyi Biotec, 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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    Image Search Results


    (A and B) Tumor growth kinetics (A) and mass (B) of WT or miR-155 TKO mice challenged with MC38 cells and administered ICI or PBS 4, 7, and 10 d.p.i. (red arrows). Data were pooled from two replicate experiments; n = 11–22; robust regression and outlier removal (ROUT) outlier test (Q = 1%). (C–P) Representative frequency and number of CD8 + T cells/g of tumor (C and D) and intratumoral frequency of Gzmb + (E and G), IFNγ + (F and H), PD-1 + (I and K), Tim-3 + (J and L), Tscm CD44 − CD62L + (M and N), CM CD44 + CD62L + (M and O), and eff CD44 + CD62L − (M and P) CD8 + T cells; n = 7–10. One-way ANOVA with multiple comparisons of means of each group; * p > 0.05, ** p > 0.01, *** p > 0.001, **** p > 0.0001. Bars represent mean; error bars represent SEM. See also .

    Journal: Cell reports

    Article Title: A microRNA-regulated transcriptional state defines intratumoral CD8 + T cells that respond to immunotherapy

    doi: 10.1016/j.celrep.2025.115301

    Figure Lengend Snippet: (A and B) Tumor growth kinetics (A) and mass (B) of WT or miR-155 TKO mice challenged with MC38 cells and administered ICI or PBS 4, 7, and 10 d.p.i. (red arrows). Data were pooled from two replicate experiments; n = 11–22; robust regression and outlier removal (ROUT) outlier test (Q = 1%). (C–P) Representative frequency and number of CD8 + T cells/g of tumor (C and D) and intratumoral frequency of Gzmb + (E and G), IFNγ + (F and H), PD-1 + (I and K), Tim-3 + (J and L), Tscm CD44 − CD62L + (M and N), CM CD44 + CD62L + (M and O), and eff CD44 + CD62L − (M and P) CD8 + T cells; n = 7–10. One-way ANOVA with multiple comparisons of means of each group; * p > 0.05, ** p > 0.01, *** p > 0.001, **** p > 0.0001. Bars represent mean; error bars represent SEM. See also .

    Article Snippet: PE/Dazzle TM 594 anti-mouse CD366 (Tim-3) Antibody (Clone #134013) , Cell Signaling , Cat#134014; RRID:AB_2632738.

    Techniques:

    Journal: Cell reports

    Article Title: A microRNA-regulated transcriptional state defines intratumoral CD8 + T cells that respond to immunotherapy

    doi: 10.1016/j.celrep.2025.115301

    Figure Lengend Snippet:

    Article Snippet: PE/Dazzle TM 594 anti-mouse CD366 (Tim-3) Antibody (Clone #134013) , Cell Signaling , Cat#134014; RRID:AB_2632738.

    Techniques: Staining, Virus, Plasmid Preparation, CRISPR, Recombinant, SYBR Green Assay, Infection, Protease Inhibitor, Isolation, Cell Isolation, Activation Assay, Gene Expression, Amplification, Software