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ct26 murine carcinoma cell line  (ATCC)


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    Structured Review

    ATCC ct26 murine carcinoma cell line
    Ct26 Murine Carcinoma Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3175 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ct26+wt+cells/CT26%2EWT/10__1158_slash_1078___0432__ccr___26___2049-113-8-17
    Average 99 stars, based on 3175 article reviews
    ct26 murine carcinoma cell line - by Bioz Stars, 2026-10
    99/100 stars

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    Cell Culture:

    Article Title: T H 17 cells regulate chemokine expression in epithelial cells through C/EBPβ and dictate host sensitivity to colitis and cancer immunity
    Article Snippet: HCT116 (ATCC, catalog no. CCL-247), MDA-MB-231 (ATCC, catalog no. HTB-26), EO771 (ATCC, catalog no. CRL-3461), and RM-1 (ATCC, catalog no. CRL-3310) cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM; Gibco) supplemented with 10% heat-inactivated fetal bovine serum (FBS). .. CT26.WT cells (ATCC, catalog no. CRL-2638) were cultured in RPMI 1640 medium (Gibco) supplemented with 10% FBS (Hyclone). .. C3.43 cells (gift from M. Kast, University of Southern California) were cultured in DMEM with 10% FBS and 0.1% 2-mercaptoethanol (Thermo Fisher Scientific, catalog no. 21985023).

    Article Title: Cyclic Peptide–Polymer Conjugate Nanotubes for Delivery of SN‐38 in Treatment of Colorectal Cancer Model
    Article Snippet: .. CT26.WT cells were acquired from the American Type Culture Collection (ATCC 2638) and cultured in Dulbecco's Modified Eagle Medium (DMEM) supplemented with foetal bovine serum (FBS, 10% v/v) and 1% Penicillin/Streptomycin (v/v) in a CO2 (5%) incubator at 37 °C. ..

    Article Title: Balancing cell cycle arrest and immune activation: A synergistic window for idasanutlin and anti-PD-1 therapy in a syngeneic mouse model.
    Article Snippet: .. B16-F10 and CT26.WT cells (American Type Culture Collection, Manassas, VA, USA), MC38 (Kerafast Inc., Boston, MU, USA), and U-2 OS (European Collection of Authenticated Cell Cultures via Sigma Aldrich, Saint Louis, MO, USA) were cultured in DMEM containing 4.5 g/L glucose (CT26.WT, MC38), RPMI-1640 (B16-F10), or McCoy’s 5 A (U-2 OS), all supplemented with 10 % FBS and L-glutamine. ..

    Article Title: Sodium Butyrate Enhances Sorafenib-Induced Ferroptosis and Immunogenic Cell Death by Modulating IRF2-Oasl2-cGAS Pathway in Colorectal Cancer
    Article Snippet: .. CT26.WT cells (ATCC, CRL-2638) were cultured in Dulbecco’s Modified Eagle Medium (DMEM; Biochannel, Nanjing, China) supplemented with 10 % (v/v) fetal bovine serum and 1 % (v/v) penicillinstreptomycin (100 IU/mL) at 37 ◦C in a humidified atmosphere containing 95 % relative humidity and 5 % CO2. .. Female Balb/c mice (5–6 weeks old, weighing 18–22 g) were obtained from GemPharmatech Co., Ltd. (Nanjing, China) to establish a subcutaneous tumor transplantation model. For tumor growth and survival analysis in vivo, 1 × 105 CT26 cells were injected subcutaneously into the flank of each Balb/c mouse.

    Article Title: Sodium butyrate enhances sorafenib-induced ferroptosis and immunogenic cell death by modulating IRF2-Oasl2-cGAS pathway in colorectal cancer
    Article Snippet: .. CT26.WT cells (ATCC, CRL-2638) were cultured in Dulbecco's Modified Eagle Medium (DMEM; Biochannel, Nanjing, China) supplemented with 10 % (v/v) fetal bovine serum and 1 % (v/v) penicillin-streptomycin (100 IU/mL) at 37 °C in a humidified atmosphere containing 95 % relative humidity and 5 % CO 2 . .. Female Balb/c mice (5–6 weeks old, weighing 18–22 g) were obtained from GemPharmatech Co., Ltd. (Nanjing, China) to establish a subcutaneous tumor transplantation model. For tumor growth and survival analysis in vivo, 1 × 10 5 CT26 cells were injected subcutaneously into the flank of each Balb/c mouse.

    Article Title: Cyclic Peptide-Polymer Conjugate Nanotubes for Delivery of SN-38 in Treatment of Colorectal Cancer Model.
    Article Snippet: .. In Vitro Testing-Cell Culture: CT26.WT cells were acquired from the American Type Culture Collection (ATCC 2638) and cultured in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with foetal bovine serum (FBS, 10% v/v) and 1% Penicillin/Streptomycin (v/v) in a CO2 (5%) incubator at 37 °C. ..

    Modification:

    Article Title: Cyclic Peptide–Polymer Conjugate Nanotubes for Delivery of SN‐38 in Treatment of Colorectal Cancer Model
    Article Snippet: .. CT26.WT cells were acquired from the American Type Culture Collection (ATCC 2638) and cultured in Dulbecco's Modified Eagle Medium (DMEM) supplemented with foetal bovine serum (FBS, 10% v/v) and 1% Penicillin/Streptomycin (v/v) in a CO2 (5%) incubator at 37 °C. ..

    Article Title: Sodium Butyrate Enhances Sorafenib-Induced Ferroptosis and Immunogenic Cell Death by Modulating IRF2-Oasl2-cGAS Pathway in Colorectal Cancer
    Article Snippet: .. CT26.WT cells (ATCC, CRL-2638) were cultured in Dulbecco’s Modified Eagle Medium (DMEM; Biochannel, Nanjing, China) supplemented with 10 % (v/v) fetal bovine serum and 1 % (v/v) penicillinstreptomycin (100 IU/mL) at 37 ◦C in a humidified atmosphere containing 95 % relative humidity and 5 % CO2. .. Female Balb/c mice (5–6 weeks old, weighing 18–22 g) were obtained from GemPharmatech Co., Ltd. (Nanjing, China) to establish a subcutaneous tumor transplantation model. For tumor growth and survival analysis in vivo, 1 × 105 CT26 cells were injected subcutaneously into the flank of each Balb/c mouse.

    Article Title: Sodium butyrate enhances sorafenib-induced ferroptosis and immunogenic cell death by modulating IRF2-Oasl2-cGAS pathway in colorectal cancer
    Article Snippet: .. CT26.WT cells (ATCC, CRL-2638) were cultured in Dulbecco's Modified Eagle Medium (DMEM; Biochannel, Nanjing, China) supplemented with 10 % (v/v) fetal bovine serum and 1 % (v/v) penicillin-streptomycin (100 IU/mL) at 37 °C in a humidified atmosphere containing 95 % relative humidity and 5 % CO 2 . .. Female Balb/c mice (5–6 weeks old, weighing 18–22 g) were obtained from GemPharmatech Co., Ltd. (Nanjing, China) to establish a subcutaneous tumor transplantation model. For tumor growth and survival analysis in vivo, 1 × 10 5 CT26 cells were injected subcutaneously into the flank of each Balb/c mouse.

    Article Title: Cyclic Peptide-Polymer Conjugate Nanotubes for Delivery of SN-38 in Treatment of Colorectal Cancer Model.
    Article Snippet: .. In Vitro Testing-Cell Culture: CT26.WT cells were acquired from the American Type Culture Collection (ATCC 2638) and cultured in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with foetal bovine serum (FBS, 10% v/v) and 1% Penicillin/Streptomycin (v/v) in a CO2 (5%) incubator at 37 °C. ..

    In Vitro:

    Article Title: Cyclic Peptide-Polymer Conjugate Nanotubes for Delivery of SN-38 in Treatment of Colorectal Cancer Model.
    Article Snippet: .. In Vitro Testing-Cell Culture: CT26.WT cells were acquired from the American Type Culture Collection (ATCC 2638) and cultured in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with foetal bovine serum (FBS, 10% v/v) and 1% Penicillin/Streptomycin (v/v) in a CO2 (5%) incubator at 37 °C. ..



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    ATCC ct26 colon carcinoma cells
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    Image Search Results


    In vitro assessment of HAase/BUF NPs-GM. ( A ) Flow cytometry analysis of Huh-7 cell uptake after incubation with the indicated formulations for 2, 6, 12, 24, 48, and 72 h. ( B ) Quantification of mean fluorescence intensity from ( A ). ( C ) Cell viability of Huh-7 cells treated with free BUF, BUF NPs, GA single load, GA dual load, No GA dual load, or No GA and HYD dual load at BUF concentrations of 0–200 nM for 72 h. ( D ) IC 5 0 values derived by nonlinear fitting. ( E ) Viability of normal THLE-2 cells treated with BUF NPs, GA single load, or GA dual load at 104.97 nM BUF for 72 h. Data are mean ± SD from three independent experiments (n = 3). **p < 0.01, *p < 0.05 vs the indicated group (one-way ANOVA with LSD post-hoc test, SPSS version 19).

    Journal: International Journal of Nanomedicine

    Article Title: Sequential-Delivery Gel Microspheres Integrating HAase-Mediated ECM Remodeling and GA-Active Targeting for Deep Tumor Penetration in TACE-Treated HCC

    doi: 10.2147/IJN.S634549

    Figure Lengend Snippet: In vitro assessment of HAase/BUF NPs-GM. ( A ) Flow cytometry analysis of Huh-7 cell uptake after incubation with the indicated formulations for 2, 6, 12, 24, 48, and 72 h. ( B ) Quantification of mean fluorescence intensity from ( A ). ( C ) Cell viability of Huh-7 cells treated with free BUF, BUF NPs, GA single load, GA dual load, No GA dual load, or No GA and HYD dual load at BUF concentrations of 0–200 nM for 72 h. ( D ) IC 5 0 values derived by nonlinear fitting. ( E ) Viability of normal THLE-2 cells treated with BUF NPs, GA single load, or GA dual load at 104.97 nM BUF for 72 h. Data are mean ± SD from three independent experiments (n = 3). **p < 0.01, *p < 0.05 vs the indicated group (one-way ANOVA with LSD post-hoc test, SPSS version 19).

    Article Snippet: Huh-7 hepatocellular carcinoma cells (BNCC337690) and normal THLE-2 liver cells (CRL-2638) were purchased from BeNa Culture Collection and ATCC, respectively.

    Techniques: In Vitro Evaluation, Flow Cytometry, Analysis, Incubation, Fluorescence, Derivative Assay