b16f10 atcc 6475 experimental models Search Results


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ATCC mouse melanoma cell b16
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ATCC crl 6475
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ATCC b16f10luc2 cells
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ATCC b16 f10
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ATCC b16f10 crl 6475 cell lines
Overexpression of IG4ΔEXT enhances the antitumor activity of CD8 + T cells in vitro and in vivo . (A) Efficiency of the retroviral transduction of EV or IG4ΔEXT in CD8 + T cells from OTI mouse. (B) EV- or IG4ΔEXT- OTI CD8 + T cells were incubated with <t>B16F10</t> in the presence or absence of OVA 257-265 for 9 h, and then the surface expression of CD69 was measured. IFN-γ and TNF-α were measured at 24 h post-incubation with B16F10 in the presence or absence of OVA peptide. * P < 0.001 vs. EV- OTI CD8 + T cells. (C) Target cells from (B) were stained with 7-AAD, and dead cells were counted by flow cytometry. (B, C) Data represent the means of three independent experiments. * P < 0.001 vs. EV- OTI CD8 + T cells (D) Schematic diagram of the metastasis and solid tumor mouse models (left). Gross and H&E staining images of B16F10 lung metastatic nodules from C57BL/6 mice administered via IV injection with PBS, EV-, or IG4ΔEXT- OTI CD8 + T cells (right). Arrowheads indicate metastatic foci. The metastatic colonies were quantified and represented as a bar graph. Data represent the means of three independent experiments (n=4 mice per group). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells. (E) Images of B16F10 solid tumors obtained from mice. Tumor volumes were measured using calipers every 3 days after PBS or T cell (EV -OTI CD8 + T, wt-IG4- OTI CD8 + T, and IG4ΔEXT- OTI CD8 + T) injection until day 21. (F) In some cases, tumors were harvested at day 14 from the mice described above (E) . Tumor weights were measured at the end of the experiments. Data are representative of four independent experiments (n=6 mice per group for each experiment). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells.
B16f10 Crl 6475 Cell Lines, supplied by ATCC, 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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ATCC mouse melanoma line
Overexpression of IG4ΔEXT enhances the antitumor activity of CD8 + T cells in vitro and in vivo . (A) Efficiency of the retroviral transduction of EV or IG4ΔEXT in CD8 + T cells from OTI mouse. (B) EV- or IG4ΔEXT- OTI CD8 + T cells were incubated with <t>B16F10</t> in the presence or absence of OVA 257-265 for 9 h, and then the surface expression of CD69 was measured. IFN-γ and TNF-α were measured at 24 h post-incubation with B16F10 in the presence or absence of OVA peptide. * P < 0.001 vs. EV- OTI CD8 + T cells. (C) Target cells from (B) were stained with 7-AAD, and dead cells were counted by flow cytometry. (B, C) Data represent the means of three independent experiments. * P < 0.001 vs. EV- OTI CD8 + T cells (D) Schematic diagram of the metastasis and solid tumor mouse models (left). Gross and H&E staining images of B16F10 lung metastatic nodules from C57BL/6 mice administered via IV injection with PBS, EV-, or IG4ΔEXT- OTI CD8 + T cells (right). Arrowheads indicate metastatic foci. The metastatic colonies were quantified and represented as a bar graph. Data represent the means of three independent experiments (n=4 mice per group). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells. (E) Images of B16F10 solid tumors obtained from mice. Tumor volumes were measured using calipers every 3 days after PBS or T cell (EV -OTI CD8 + T, wt-IG4- OTI CD8 + T, and IG4ΔEXT- OTI CD8 + T) injection until day 21. (F) In some cases, tumors were harvested at day 14 from the mice described above (E) . Tumor weights were measured at the end of the experiments. Data are representative of four independent experiments (n=6 mice per group for each experiment). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells.
Mouse Melanoma Line, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC eukaryotic cell lines
Overexpression of IG4ΔEXT enhances the antitumor activity of CD8 + T cells in vitro and in vivo . (A) Efficiency of the retroviral transduction of EV or IG4ΔEXT in CD8 + T cells from OTI mouse. (B) EV- or IG4ΔEXT- OTI CD8 + T cells were incubated with <t>B16F10</t> in the presence or absence of OVA 257-265 for 9 h, and then the surface expression of CD69 was measured. IFN-γ and TNF-α were measured at 24 h post-incubation with B16F10 in the presence or absence of OVA peptide. * P < 0.001 vs. EV- OTI CD8 + T cells. (C) Target cells from (B) were stained with 7-AAD, and dead cells were counted by flow cytometry. (B, C) Data represent the means of three independent experiments. * P < 0.001 vs. EV- OTI CD8 + T cells (D) Schematic diagram of the metastasis and solid tumor mouse models (left). Gross and H&E staining images of B16F10 lung metastatic nodules from C57BL/6 mice administered via IV injection with PBS, EV-, or IG4ΔEXT- OTI CD8 + T cells (right). Arrowheads indicate metastatic foci. The metastatic colonies were quantified and represented as a bar graph. Data represent the means of three independent experiments (n=4 mice per group). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells. (E) Images of B16F10 solid tumors obtained from mice. Tumor volumes were measured using calipers every 3 days after PBS or T cell (EV -OTI CD8 + T, wt-IG4- OTI CD8 + T, and IG4ΔEXT- OTI CD8 + T) injection until day 21. (F) In some cases, tumors were harvested at day 14 from the mice described above (E) . Tumor weights were measured at the end of the experiments. Data are representative of four independent experiments (n=6 mice per group for each experiment). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells.
Eukaryotic Cell Lines, supplied by ATCC, 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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ATCC crl 6475 crl 2639
Overexpression of IG4ΔEXT enhances the antitumor activity of CD8 + T cells in vitro and in vivo . (A) Efficiency of the retroviral transduction of EV or IG4ΔEXT in CD8 + T cells from OTI mouse. (B) EV- or IG4ΔEXT- OTI CD8 + T cells were incubated with <t>B16F10</t> in the presence or absence of OVA 257-265 for 9 h, and then the surface expression of CD69 was measured. IFN-γ and TNF-α were measured at 24 h post-incubation with B16F10 in the presence or absence of OVA peptide. * P < 0.001 vs. EV- OTI CD8 + T cells. (C) Target cells from (B) were stained with 7-AAD, and dead cells were counted by flow cytometry. (B, C) Data represent the means of three independent experiments. * P < 0.001 vs. EV- OTI CD8 + T cells (D) Schematic diagram of the metastasis and solid tumor mouse models (left). Gross and H&E staining images of B16F10 lung metastatic nodules from C57BL/6 mice administered via IV injection with PBS, EV-, or IG4ΔEXT- OTI CD8 + T cells (right). Arrowheads indicate metastatic foci. The metastatic colonies were quantified and represented as a bar graph. Data represent the means of three independent experiments (n=4 mice per group). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells. (E) Images of B16F10 solid tumors obtained from mice. Tumor volumes were measured using calipers every 3 days after PBS or T cell (EV -OTI CD8 + T, wt-IG4- OTI CD8 + T, and IG4ΔEXT- OTI CD8 + T) injection until day 21. (F) In some cases, tumors were harvested at day 14 from the mice described above (E) . Tumor weights were measured at the end of the experiments. Data are representative of four independent experiments (n=6 mice per group for each experiment). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells.
Crl 6475 Crl 2639, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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LGC Promochem b16f10 cells # crl-6475
Overexpression of IG4ΔEXT enhances the antitumor activity of CD8 + T cells in vitro and in vivo . (A) Efficiency of the retroviral transduction of EV or IG4ΔEXT in CD8 + T cells from OTI mouse. (B) EV- or IG4ΔEXT- OTI CD8 + T cells were incubated with <t>B16F10</t> in the presence or absence of OVA 257-265 for 9 h, and then the surface expression of CD69 was measured. IFN-γ and TNF-α were measured at 24 h post-incubation with B16F10 in the presence or absence of OVA peptide. * P < 0.001 vs. EV- OTI CD8 + T cells. (C) Target cells from (B) were stained with 7-AAD, and dead cells were counted by flow cytometry. (B, C) Data represent the means of three independent experiments. * P < 0.001 vs. EV- OTI CD8 + T cells (D) Schematic diagram of the metastasis and solid tumor mouse models (left). Gross and H&E staining images of B16F10 lung metastatic nodules from C57BL/6 mice administered via IV injection with PBS, EV-, or IG4ΔEXT- OTI CD8 + T cells (right). Arrowheads indicate metastatic foci. The metastatic colonies were quantified and represented as a bar graph. Data represent the means of three independent experiments (n=4 mice per group). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells. (E) Images of B16F10 solid tumors obtained from mice. Tumor volumes were measured using calipers every 3 days after PBS or T cell (EV -OTI CD8 + T, wt-IG4- OTI CD8 + T, and IG4ΔEXT- OTI CD8 + T) injection until day 21. (F) In some cases, tumors were harvested at day 14 from the mice described above (E) . Tumor weights were measured at the end of the experiments. Data are representative of four independent experiments (n=6 mice per group for each experiment). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells.
B16f10 Cells # Crl 6475, supplied by LGC Promochem, 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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ATCC 6475 mcf7 human breast carcinoma atcc cat
Overexpression of IG4ΔEXT enhances the antitumor activity of CD8 + T cells in vitro and in vivo . (A) Efficiency of the retroviral transduction of EV or IG4ΔEXT in CD8 + T cells from OTI mouse. (B) EV- or IG4ΔEXT- OTI CD8 + T cells were incubated with <t>B16F10</t> in the presence or absence of OVA 257-265 for 9 h, and then the surface expression of CD69 was measured. IFN-γ and TNF-α were measured at 24 h post-incubation with B16F10 in the presence or absence of OVA peptide. * P < 0.001 vs. EV- OTI CD8 + T cells. (C) Target cells from (B) were stained with 7-AAD, and dead cells were counted by flow cytometry. (B, C) Data represent the means of three independent experiments. * P < 0.001 vs. EV- OTI CD8 + T cells (D) Schematic diagram of the metastasis and solid tumor mouse models (left). Gross and H&E staining images of B16F10 lung metastatic nodules from C57BL/6 mice administered via IV injection with PBS, EV-, or IG4ΔEXT- OTI CD8 + T cells (right). Arrowheads indicate metastatic foci. The metastatic colonies were quantified and represented as a bar graph. Data represent the means of three independent experiments (n=4 mice per group). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells. (E) Images of B16F10 solid tumors obtained from mice. Tumor volumes were measured using calipers every 3 days after PBS or T cell (EV -OTI CD8 + T, wt-IG4- OTI CD8 + T, and IG4ΔEXT- OTI CD8 + T) injection until day 21. (F) In some cases, tumors were harvested at day 14 from the mice described above (E) . Tumor weights were measured at the end of the experiments. Data are representative of four independent experiments (n=6 mice per group for each experiment). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells.
6475 Mcf7 Human Breast Carcinoma Atcc Cat, supplied by ATCC, 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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ATCC cell lines b16 f0 atcc crl 6322 b16 f10 atcc crl 6475 ln lines
Overexpression of IG4ΔEXT enhances the antitumor activity of CD8 + T cells in vitro and in vivo . (A) Efficiency of the retroviral transduction of EV or IG4ΔEXT in CD8 + T cells from OTI mouse. (B) EV- or IG4ΔEXT- OTI CD8 + T cells were incubated with <t>B16F10</t> in the presence or absence of OVA 257-265 for 9 h, and then the surface expression of CD69 was measured. IFN-γ and TNF-α were measured at 24 h post-incubation with B16F10 in the presence or absence of OVA peptide. * P < 0.001 vs. EV- OTI CD8 + T cells. (C) Target cells from (B) were stained with 7-AAD, and dead cells were counted by flow cytometry. (B, C) Data represent the means of three independent experiments. * P < 0.001 vs. EV- OTI CD8 + T cells (D) Schematic diagram of the metastasis and solid tumor mouse models (left). Gross and H&E staining images of B16F10 lung metastatic nodules from C57BL/6 mice administered via IV injection with PBS, EV-, or IG4ΔEXT- OTI CD8 + T cells (right). Arrowheads indicate metastatic foci. The metastatic colonies were quantified and represented as a bar graph. Data represent the means of three independent experiments (n=4 mice per group). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells. (E) Images of B16F10 solid tumors obtained from mice. Tumor volumes were measured using calipers every 3 days after PBS or T cell (EV -OTI CD8 + T, wt-IG4- OTI CD8 + T, and IG4ΔEXT- OTI CD8 + T) injection until day 21. (F) In some cases, tumors were harvested at day 14 from the mice described above (E) . Tumor weights were measured at the end of the experiments. Data are representative of four independent experiments (n=6 mice per group for each experiment). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells.
Cell Lines B16 F0 Atcc Crl 6322 B16 F10 Atcc Crl 6475 Ln Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Overexpression of IG4ΔEXT enhances the antitumor activity of CD8 + T cells in vitro and in vivo . (A) Efficiency of the retroviral transduction of EV or IG4ΔEXT in CD8 + T cells from OTI mouse. (B) EV- or IG4ΔEXT- OTI CD8 + T cells were incubated with B16F10 in the presence or absence of OVA 257-265 for 9 h, and then the surface expression of CD69 was measured. IFN-γ and TNF-α were measured at 24 h post-incubation with B16F10 in the presence or absence of OVA peptide. * P < 0.001 vs. EV- OTI CD8 + T cells. (C) Target cells from (B) were stained with 7-AAD, and dead cells were counted by flow cytometry. (B, C) Data represent the means of three independent experiments. * P < 0.001 vs. EV- OTI CD8 + T cells (D) Schematic diagram of the metastasis and solid tumor mouse models (left). Gross and H&E staining images of B16F10 lung metastatic nodules from C57BL/6 mice administered via IV injection with PBS, EV-, or IG4ΔEXT- OTI CD8 + T cells (right). Arrowheads indicate metastatic foci. The metastatic colonies were quantified and represented as a bar graph. Data represent the means of three independent experiments (n=4 mice per group). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells. (E) Images of B16F10 solid tumors obtained from mice. Tumor volumes were measured using calipers every 3 days after PBS or T cell (EV -OTI CD8 + T, wt-IG4- OTI CD8 + T, and IG4ΔEXT- OTI CD8 + T) injection until day 21. (F) In some cases, tumors were harvested at day 14 from the mice described above (E) . Tumor weights were measured at the end of the experiments. Data are representative of four independent experiments (n=6 mice per group for each experiment). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells.

Journal: Frontiers in Immunology

Article Title: Potentiating the Antitumor Activity of Cytotoxic T Cells via the Transmembrane Domain of IGSF4 That Increases TCR Avidity

doi: 10.3389/fimmu.2020.591054

Figure Lengend Snippet: Overexpression of IG4ΔEXT enhances the antitumor activity of CD8 + T cells in vitro and in vivo . (A) Efficiency of the retroviral transduction of EV or IG4ΔEXT in CD8 + T cells from OTI mouse. (B) EV- or IG4ΔEXT- OTI CD8 + T cells were incubated with B16F10 in the presence or absence of OVA 257-265 for 9 h, and then the surface expression of CD69 was measured. IFN-γ and TNF-α were measured at 24 h post-incubation with B16F10 in the presence or absence of OVA peptide. * P < 0.001 vs. EV- OTI CD8 + T cells. (C) Target cells from (B) were stained with 7-AAD, and dead cells were counted by flow cytometry. (B, C) Data represent the means of three independent experiments. * P < 0.001 vs. EV- OTI CD8 + T cells (D) Schematic diagram of the metastasis and solid tumor mouse models (left). Gross and H&E staining images of B16F10 lung metastatic nodules from C57BL/6 mice administered via IV injection with PBS, EV-, or IG4ΔEXT- OTI CD8 + T cells (right). Arrowheads indicate metastatic foci. The metastatic colonies were quantified and represented as a bar graph. Data represent the means of three independent experiments (n=4 mice per group). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells. (E) Images of B16F10 solid tumors obtained from mice. Tumor volumes were measured using calipers every 3 days after PBS or T cell (EV -OTI CD8 + T, wt-IG4- OTI CD8 + T, and IG4ΔEXT- OTI CD8 + T) injection until day 21. (F) In some cases, tumors were harvested at day 14 from the mice described above (E) . Tumor weights were measured at the end of the experiments. Data are representative of four independent experiments (n=6 mice per group for each experiment). * P < 0.005 vs. PBS, ** P < 0.001 vs. EV- OTI CD8 + T cells.

Article Snippet: Jurkat T (TIB-152), HEK293T (CRL-1573), and B16F10 (CRL-6475) cell lines were purchased from ATCC.

Techniques: Over Expression, Activity Assay, In Vitro, In Vivo, Retroviral, Transduction, Incubation, Expressing, Staining, Flow Cytometry, IV Injection, Injection