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cho k1 cell line  (ATCC)


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    Structured Review

    ATCC cho k1 cell line
    Cho K1 Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 7374 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cho k1 cell line/product/ATCC
    Average 99 stars, based on 7374 article reviews
    cho k1 cell line - by Bioz Stars, 2026-05
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    Viability of CHO-K1 cells after 24 h of treatment with D. superbus ( A ) and P. paradoxus ( B ) expressed as a percentage of the DMSO control (set to 100%). Data are presented as mean ± STD from three independent experiments.

    Journal: Scientific Reports

    Article Title: Genotoxic potential of Dianthus superbus var. superbus and Petasites paradoxus (Retz.) Baumg. methanolic extracts in Chinese hamster ovary cells

    doi: 10.1038/s41598-026-50267-x

    Figure Lengend Snippet: Viability of CHO-K1 cells after 24 h of treatment with D. superbus ( A ) and P. paradoxus ( B ) expressed as a percentage of the DMSO control (set to 100%). Data are presented as mean ± STD from three independent experiments.

    Article Snippet: The CHO-K1 cell line (603480) was purchased from CLS Cell Lines Service (GmbH, Germany).

    Techniques: Control

    The cytotoxic effects of D. superbus extracts ( A ) and P. paradoxus ( B ) extracts on CHO-K1 cells under the CBMN assay in the absence and presence of MMC. Data represents the mean values from three independent experiments.

    Journal: Scientific Reports

    Article Title: Genotoxic potential of Dianthus superbus var. superbus and Petasites paradoxus (Retz.) Baumg. methanolic extracts in Chinese hamster ovary cells

    doi: 10.1038/s41598-026-50267-x

    Figure Lengend Snippet: The cytotoxic effects of D. superbus extracts ( A ) and P. paradoxus ( B ) extracts on CHO-K1 cells under the CBMN assay in the absence and presence of MMC. Data represents the mean values from three independent experiments.

    Article Snippet: The CHO-K1 cell line (603480) was purchased from CLS Cell Lines Service (GmbH, Germany).

    Techniques:

    ( A ) The effect of different D. superbus extract treatments on the micronuclei frequency (%) in CHO-K1 cells. Cells were treated for 24 h either with DMSO at 0.3% (NC), MMC at 0.025 µg/mL or 3 different concentrations of D. superbus extract, 6.3, 12.5 and 25 µg/mL. Then cells were incubated with 3 µg/mL of cytochalasin B for another 24 h. Graphs represent data collected from 3 independent experiments. One-way ANOVA, Tukey’s multiple comparisons test using GraphPad Prism 7 software, was applied to calculate statistical significance in comparison with the NC control. (* p = 0.0155, *** p = 0.0006, **** p < 0.0001). Micronuclei frequency (%) was calculated from the following Equation: Micronuclei frequency (%) = binucleated cells with MN /binucleated cells *100. ( B ) Representative microscopic images showing micronuclei formation in binucleated CHO-K1 cells, observed with a 40× objective. CHO-K1 cell DNA was stained with Hoechst dye. Green arrows indicate the micronuclei, and the white line, labelled 50 μm, represents the scale bar in the image.

    Journal: Scientific Reports

    Article Title: Genotoxic potential of Dianthus superbus var. superbus and Petasites paradoxus (Retz.) Baumg. methanolic extracts in Chinese hamster ovary cells

    doi: 10.1038/s41598-026-50267-x

    Figure Lengend Snippet: ( A ) The effect of different D. superbus extract treatments on the micronuclei frequency (%) in CHO-K1 cells. Cells were treated for 24 h either with DMSO at 0.3% (NC), MMC at 0.025 µg/mL or 3 different concentrations of D. superbus extract, 6.3, 12.5 and 25 µg/mL. Then cells were incubated with 3 µg/mL of cytochalasin B for another 24 h. Graphs represent data collected from 3 independent experiments. One-way ANOVA, Tukey’s multiple comparisons test using GraphPad Prism 7 software, was applied to calculate statistical significance in comparison with the NC control. (* p = 0.0155, *** p = 0.0006, **** p < 0.0001). Micronuclei frequency (%) was calculated from the following Equation: Micronuclei frequency (%) = binucleated cells with MN /binucleated cells *100. ( B ) Representative microscopic images showing micronuclei formation in binucleated CHO-K1 cells, observed with a 40× objective. CHO-K1 cell DNA was stained with Hoechst dye. Green arrows indicate the micronuclei, and the white line, labelled 50 μm, represents the scale bar in the image.

    Article Snippet: The CHO-K1 cell line (603480) was purchased from CLS Cell Lines Service (GmbH, Germany).

    Techniques: Incubation, Software, Comparison, Control, Staining

    ( A ) The effect of different D. superbus extract treatments on the micronuclei frequency (%) in CHO-K1 cells in the presence of MMC. Cells were treated for 24 h either with DMSO (NC), MMC at 0.025 µg/mL or in combnation of MMC and of D. superbus extract at 3 different concentrations 6.3, 12.5 and 25 µg/mL 24 h, then incubation with 3 µg/mL of cytochalasin B for another 24 h. Graphs represent data collected from 3 independent experiments. One-way ANOVA, Tukey’s multiple comparisons test using GraphPad Prism 7 software, was applied to calculate statistical significance in comparison with the NC control. (* p = 0.0155, *** p = 0.0006, **** p < 0.0001). Micronuclei frequency (%) was calculated from the following Equation: Micronuclei frequency (%) = binucleated cells with MN /binucleated cells *100. ( B ) Representative images illustrating micronuclei formation in binucleated CHO-K1 cells after exposure to MMC alone or in combination with the highest tested concentration of D. superbus extract.

    Journal: Scientific Reports

    Article Title: Genotoxic potential of Dianthus superbus var. superbus and Petasites paradoxus (Retz.) Baumg. methanolic extracts in Chinese hamster ovary cells

    doi: 10.1038/s41598-026-50267-x

    Figure Lengend Snippet: ( A ) The effect of different D. superbus extract treatments on the micronuclei frequency (%) in CHO-K1 cells in the presence of MMC. Cells were treated for 24 h either with DMSO (NC), MMC at 0.025 µg/mL or in combnation of MMC and of D. superbus extract at 3 different concentrations 6.3, 12.5 and 25 µg/mL 24 h, then incubation with 3 µg/mL of cytochalasin B for another 24 h. Graphs represent data collected from 3 independent experiments. One-way ANOVA, Tukey’s multiple comparisons test using GraphPad Prism 7 software, was applied to calculate statistical significance in comparison with the NC control. (* p = 0.0155, *** p = 0.0006, **** p < 0.0001). Micronuclei frequency (%) was calculated from the following Equation: Micronuclei frequency (%) = binucleated cells with MN /binucleated cells *100. ( B ) Representative images illustrating micronuclei formation in binucleated CHO-K1 cells after exposure to MMC alone or in combination with the highest tested concentration of D. superbus extract.

    Article Snippet: The CHO-K1 cell line (603480) was purchased from CLS Cell Lines Service (GmbH, Germany).

    Techniques: Incubation, Software, Comparison, Control, Concentration Assay

    ( A ) The effect of different P. paradoxus extract treatments on the micronuclei frequency (%) in CHO-K1 cells. Cells were treated for 24 h with 3 different concentrations of P. paradoxus extract, 12.5, 25 and 50 µg/mL or MMC at 0.025 µg/mL, then followed by 24 h incubation with 3 µg/mL of cytochalasin B. Graphs represent data collected from 3 independent experiments. One-way ANOVA, Tukey’s multiple comparisons test using GraphPad Prism 7 software, was applied to calculate statistical significance in comparison with the NC control. (* p = 0.0435, ** p = 0.0019, *** p = 0.0007, **** p < 0.0001). ( B ) The micronuclei formation in binucleated CHO-K1 cells, observed with a 40× objective. CHO-K1 cells’ DNA was stained with Hoechst dye. Green arrows indicate the micronuclei, and the white line, labelled 50 μm, represents the scale bar in the image.

    Journal: Scientific Reports

    Article Title: Genotoxic potential of Dianthus superbus var. superbus and Petasites paradoxus (Retz.) Baumg. methanolic extracts in Chinese hamster ovary cells

    doi: 10.1038/s41598-026-50267-x

    Figure Lengend Snippet: ( A ) The effect of different P. paradoxus extract treatments on the micronuclei frequency (%) in CHO-K1 cells. Cells were treated for 24 h with 3 different concentrations of P. paradoxus extract, 12.5, 25 and 50 µg/mL or MMC at 0.025 µg/mL, then followed by 24 h incubation with 3 µg/mL of cytochalasin B. Graphs represent data collected from 3 independent experiments. One-way ANOVA, Tukey’s multiple comparisons test using GraphPad Prism 7 software, was applied to calculate statistical significance in comparison with the NC control. (* p = 0.0435, ** p = 0.0019, *** p = 0.0007, **** p < 0.0001). ( B ) The micronuclei formation in binucleated CHO-K1 cells, observed with a 40× objective. CHO-K1 cells’ DNA was stained with Hoechst dye. Green arrows indicate the micronuclei, and the white line, labelled 50 μm, represents the scale bar in the image.

    Article Snippet: The CHO-K1 cell line (603480) was purchased from CLS Cell Lines Service (GmbH, Germany).

    Techniques: Incubation, Software, Comparison, Control, Staining

    ( A ) The effect of different P. paradoxus extract treatments on the micronuclei frequency (%) in CHO-K1 cells. Cells were treated for 24 h with 3 different concentrations of P. paradoxus extract, in the presence of MMC, then followed by 24 h of incubation with 3 µg/mL of cytochalasin B. Graphs represent data collected from 3 independent experiments. One-way ANOVA, Tukey’s multiple comparisons test using GraphPad Prism 7 software, was applied to calculate statistical significance in comparison with NC control. (* p = 0.0435, ** p = 0.0019, *** p = 0.0007, **** p < 0.0001). in micronuclei frequency (%) was calculated from the following Equation: ( B ) Representative microscopic images showing micronuclei formation in binucleated CHO-K1 cells, observed with a 40× objective after 24 treated with 0.025 µg/mL MMC alone or MMC + P. paradoxus extract at 25 µg/mL. CHO-K1 cell DNA was stained with Hoechst dye. Green arrows indicate the micronuclei, and the white line, labelled 50 μm, represents the scale bar in the image.

    Journal: Scientific Reports

    Article Title: Genotoxic potential of Dianthus superbus var. superbus and Petasites paradoxus (Retz.) Baumg. methanolic extracts in Chinese hamster ovary cells

    doi: 10.1038/s41598-026-50267-x

    Figure Lengend Snippet: ( A ) The effect of different P. paradoxus extract treatments on the micronuclei frequency (%) in CHO-K1 cells. Cells were treated for 24 h with 3 different concentrations of P. paradoxus extract, in the presence of MMC, then followed by 24 h of incubation with 3 µg/mL of cytochalasin B. Graphs represent data collected from 3 independent experiments. One-way ANOVA, Tukey’s multiple comparisons test using GraphPad Prism 7 software, was applied to calculate statistical significance in comparison with NC control. (* p = 0.0435, ** p = 0.0019, *** p = 0.0007, **** p < 0.0001). in micronuclei frequency (%) was calculated from the following Equation: ( B ) Representative microscopic images showing micronuclei formation in binucleated CHO-K1 cells, observed with a 40× objective after 24 treated with 0.025 µg/mL MMC alone or MMC + P. paradoxus extract at 25 µg/mL. CHO-K1 cell DNA was stained with Hoechst dye. Green arrows indicate the micronuclei, and the white line, labelled 50 μm, represents the scale bar in the image.

    Article Snippet: The CHO-K1 cell line (603480) was purchased from CLS Cell Lines Service (GmbH, Germany).

    Techniques: Incubation, Software, Comparison, Control, Staining