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mouse colon carcinoma cell line ct26 wt  (ATCC)


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    ATCC mouse colon carcinoma cell line ct26 wt
    Mouse Colon Carcinoma Cell Line Ct26 Wt, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3144 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+colon+carcinoma+cell+line+ct26/CT26%2EWT/pmc13201902-60-12-21
    Average 99 stars, based on 3144 article reviews
    mouse colon carcinoma cell line ct26 wt - by Bioz Stars, 2026-10
    99/100 stars

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    Cell Culture:

    Article Title: Interleukin-17F suppressed colon cancer by enhancing caspase 4 mediated pyroptosis of endothelial cells
    Article Snippet: .. The mouse colon carcinoma cell line CT26 and mouse endothelial cell line EOMA were obtained from the American Type Culture Collection and cultured in DMEM (GIBCO) supplemented with 10% FCS. .. Mouse IL-17F cDNA with HA tag was from Sino Biological Inc. (Beijing, China).

    Article Title: Enhanced anti-cancer efficacy of arginine deaminase expressed by tumor-seeking Salmonella Gallinarum
    Article Snippet: .. Cell lines and cell culture Human embryo kidney cell 293 [HEK-293], mouse breast cancer cell line 4T1, mouse colon carcinoma cell line CT26, and mouse melanoma cell line B16-F10 were all purchased from the American Type Culture Collection (ATCC). .. All cell lines were maintained in the recommended medium (HyClone, Logan, USA) containing 10% heat-inactivated fetal bovine serum (HyClone, Logan, USA) and 1% penicillin/streptomycin (HyClone, Logan, USA) in a humidi ed (37°C, 5% CO2) incubator.

    Article Title: Enhanced anti-cancer efficacy of arginine deaminase expressed by tumor-seeking Salmonella Gallinarum.
    Article Snippet: Amino acid deprivation, particularly of nonessential amino acids that can be synthesized by normal cells but not by cancer cells with specific defects in the biosynthesis pathway, has emerged as a potential strategy in cancer therapeutics.. In normal cells, arginine is synthesized from citrulline in two steps via two enzymes: argininosuccinate synthetase (ASS1) and argininosuccinate lyase.. Several cancer cells exhibit arginine auxotrophy due to the loss or down-regulation of ASS1.

    Retroviral:

    Article Title: Plasma membrane-coated nanoparticles and membrane vesicles to orchestrate multimodal antitumor immunity
    Article Snippet: .. The PG13 retroviral packaging cell line, ovarian 6 cancer cell line TOV21G, oral squamous carcinoma cell line HSC-3, mouse lymphoma cell line 7 A20, mouse colon carcinoma cell line CT26, myeloma cell line MM.1S, and leukemia cell line 8 THP-1 were purchased from the American Type Culture Collection (ATCC) (Manassas, VA). ..



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    ATCC colon carcinoma cell line ct26
    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse <t>CT26</t> tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.
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    ATCC ct26 colon carcinoma cell line
    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse <t>CT26</t> tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.
    Ct26 Colon Carcinoma Cell Line, 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
    https://www.bioz.com/product/mouse+colon+carcinoma+cell+line+ct26/CT26%2EWT%3B+Colon+Carcinoma%3B+Mouse/pm41205600-291-74-83
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    ATCC ct26 mouse colon carcinoma cell line
    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse <t>CT26</t> tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.
    Ct26 Mouse Colon Carcinoma Cell Line, 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
    https://www.bioz.com/product/mouse+colon+carcinoma+cell+line+ct26/CT26%2EWT%3B+Colon+Carcinoma%3B+Mouse/pm41174383-161-1-10
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    Image Search Results


    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse CT26 tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.

    Journal: Cell Reports Medicine

    Article Title: DF6215, an α-optimized IL-2-Fc fusion, expands immune effectors and drives robust preclinical anti-tumor activity

    doi: 10.1016/j.xcrm.2025.102518

    Figure Lengend Snippet: DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse CT26 tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.

    Article Snippet: The mouse melanoma cell line B16F10 and colon carcinoma cell line CT26 were obtained from ATCC.

    Techniques: Activity Assay, Control, Cell Characterization, Luminex

    DF6215 treatment augments anti-tumor activity compared to a non-⍺ IL-2-Fc (A) Efficacy of DF6215 monotherapy vs. non-⍺ IL-2 Fc monotherapy administered i.p. in the mouse CT26 tumor model. Individual tumor volumes are shown with treatment days and frequencies as indicated (vertical dotted lines). The number of complete responders (CRs) in each treatment group is noted in each image. N = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (∗∗∗ p < 0.001, ∗∗ p < 0.01, and ∗ p < 0.05; log rank Mantel-Cox test). Some of the DF6215 monotherapy data presented in to illustrate the dose response are included here to allow direct comparison with the non-α-binding IL-2-Fc, which was included as a comparator in the same experiment. See also . (B–D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of hIgG1 isotype, DF6215 (0.675 mg/kg), or non-⍺ IL-2-Fc (0.675 mg/kg). (B) The effector cell ratios of cells in the tumor microenvironment 96 h post-treatment (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test). (C) Frequencies of CD69 + NK and CD8 + T cells in the tumor microenvironment 48 h post-treatment. (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test). (D) Frequencies of granzyme B + NK cells and CD8 + T cells in the tumor microenvironment 48 h post-treatment (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test).

    Journal: Cell Reports Medicine

    Article Title: DF6215, an α-optimized IL-2-Fc fusion, expands immune effectors and drives robust preclinical anti-tumor activity

    doi: 10.1016/j.xcrm.2025.102518

    Figure Lengend Snippet: DF6215 treatment augments anti-tumor activity compared to a non-⍺ IL-2-Fc (A) Efficacy of DF6215 monotherapy vs. non-⍺ IL-2 Fc monotherapy administered i.p. in the mouse CT26 tumor model. Individual tumor volumes are shown with treatment days and frequencies as indicated (vertical dotted lines). The number of complete responders (CRs) in each treatment group is noted in each image. N = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (∗∗∗ p < 0.001, ∗∗ p < 0.01, and ∗ p < 0.05; log rank Mantel-Cox test). Some of the DF6215 monotherapy data presented in to illustrate the dose response are included here to allow direct comparison with the non-α-binding IL-2-Fc, which was included as a comparator in the same experiment. See also . (B–D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of hIgG1 isotype, DF6215 (0.675 mg/kg), or non-⍺ IL-2-Fc (0.675 mg/kg). (B) The effector cell ratios of cells in the tumor microenvironment 96 h post-treatment (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test). (C) Frequencies of CD69 + NK and CD8 + T cells in the tumor microenvironment 48 h post-treatment. (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test). (D) Frequencies of granzyme B + NK cells and CD8 + T cells in the tumor microenvironment 48 h post-treatment (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test).

    Article Snippet: The mouse melanoma cell line B16F10 and colon carcinoma cell line CT26 were obtained from ATCC.

    Techniques: Activity Assay, Comparison, Binding Assay