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hct116 cells  (AMS Biotechnology)


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    AMS Biotechnology hct116 cells
    Hct116 Cells, supplied by AMS Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ep-cl-0096/pm41744740-55-4-27?v=AMS+Biotechnology
    Average 96 stars, based on 2 article reviews
    hct116 cells - by Bioz Stars, 2026-07
    96/100 stars

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    AMS Biotechnology hct116 colorectal cancer cells
    Figure 3. In vitro cytotoxicity of study formulations on Caco-2 (a) and <t>HCT116</t> (b) intestinal epithelial cells. Formulations were applied to cells at a polymer concentration of 0.5 mg/mL diluted in Dulbecco’s Modified Eagle Medium (DMEM) containing 10% Fetal Bovine Serum (FBS) for 48 h. A total of 1% (v/v) Triton X-100 (TX-100) was used as the positive cell death control. Caco-2 and HCT116 cells were seeded on 96 well plates at a density of 1 × 104 and 2 × 104 cells/well, respectively, and were cultured for 24 h prior to assaying. Metabolic activity was assessed using the PrestoBlue assay. The data represent mean ± S.D. (n = 3).
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    Figure 3. In vitro cytotoxicity of study formulations on Caco-2 (a) and HCT116 (b) intestinal epithelial cells. Formulations were applied to cells at a polymer concentration of 0.5 mg/mL diluted in Dulbecco’s Modified Eagle Medium (DMEM) containing 10% Fetal Bovine Serum (FBS) for 48 h. A total of 1% (v/v) Triton X-100 (TX-100) was used as the positive cell death control. Caco-2 and HCT116 cells were seeded on 96 well plates at a density of 1 × 104 and 2 × 104 cells/well, respectively, and were cultured for 24 h prior to assaying. Metabolic activity was assessed using the PrestoBlue assay. The data represent mean ± S.D. (n = 3).

    Journal: Coatings

    Article Title: Starch/Poly(glycerol-adipate) Nanocomposites: A Novel Oral Drug Delivery Device

    doi: 10.3390/coatings10020125

    Figure Lengend Snippet: Figure 3. In vitro cytotoxicity of study formulations on Caco-2 (a) and HCT116 (b) intestinal epithelial cells. Formulations were applied to cells at a polymer concentration of 0.5 mg/mL diluted in Dulbecco’s Modified Eagle Medium (DMEM) containing 10% Fetal Bovine Serum (FBS) for 48 h. A total of 1% (v/v) Triton X-100 (TX-100) was used as the positive cell death control. Caco-2 and HCT116 cells were seeded on 96 well plates at a density of 1 × 104 and 2 × 104 cells/well, respectively, and were cultured for 24 h prior to assaying. Metabolic activity was assessed using the PrestoBlue assay. The data represent mean ± S.D. (n = 3).

    Article Snippet: Caco-2 human epithelial colorectal adenocarcinoma cells were obtained from the American Type Culture Collection (ATCC; Manassas, VA, USA), and were used between passages 30-35 and HCT116 colorectal cancer cells were obtained from AMS Biotechnology (Abingdon, UK).

    Techniques: In Vitro, Polymer, Concentration Assay, Control, Cell Culture, Activity Assay, Prestoblue Assay