breast cancer cell line zr 75 1 Search Results


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  • 93
    ATCC breast cancer cell lines zr
    Breast Cancer Cell Lines Zr, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC molecular marker 100 1500 bp
    Molecular Marker 100 1500 Bp, 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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    Thermo Fisher zr 75 1 breast cancer cells
    Cytotoxicity of metformin in HeLa and <t>ZR-75-1</t> cells. a and b HeLa cells ( a ) and ZR-75-1 ( b ) cells were treated with the indicated concentration of metformin for 35 h and 70 h, respectively. Cell viability was measured using the MTT method. c HeLa and ZR-75-1 cells were incubated with indicated concentration of metformin for 20 h and 25 h, respectively. Cell lysates were subjected to western blot analysis using antibodies against cyclin D1, cyclin B1 and H3P. ACTN was the protein loading control. The protein levels of cyclin D1, cyclin B1 and H3P after normalization with the loading control protein ACTN are presented as fold change. d HeLa and ZR-75-1 cells were incubated with the indicated concentration of metformin for 30 h and 57 h, respectively. The cells were then subjected to flow cytometric cell cycle profile analysis. The results are representative of three independent experiments
    Zr 75 1 Breast Cancer Cells, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore zr 75 1 human breast carcinoma
    Cytotoxicity of metformin in HeLa and <t>ZR-75-1</t> cells. a and b HeLa cells ( a ) and ZR-75-1 ( b ) cells were treated with the indicated concentration of metformin for 35 h and 70 h, respectively. Cell viability was measured using the MTT method. c HeLa and ZR-75-1 cells were incubated with indicated concentration of metformin for 20 h and 25 h, respectively. Cell lysates were subjected to western blot analysis using antibodies against cyclin D1, cyclin B1 and H3P. ACTN was the protein loading control. The protein levels of cyclin D1, cyclin B1 and H3P after normalization with the loading control protein ACTN are presented as fold change. d HeLa and ZR-75-1 cells were incubated with the indicated concentration of metformin for 30 h and 57 h, respectively. The cells were then subjected to flow cytometric cell cycle profile analysis. The results are representative of three independent experiments
    Zr 75 1 Human Breast Carcinoma, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Corning Life Sciences zr 75 1 breast cancer cells
    Cytotoxicity of metformin in HeLa and <t>ZR-75-1</t> cells. a and b HeLa cells ( a ) and ZR-75-1 ( b ) cells were treated with the indicated concentration of metformin for 35 h and 70 h, respectively. Cell viability was measured using the MTT method. c HeLa and ZR-75-1 cells were incubated with indicated concentration of metformin for 20 h and 25 h, respectively. Cell lysates were subjected to western blot analysis using antibodies against cyclin D1, cyclin B1 and H3P. ACTN was the protein loading control. The protein levels of cyclin D1, cyclin B1 and H3P after normalization with the loading control protein ACTN are presented as fold change. d HeLa and ZR-75-1 cells were incubated with the indicated concentration of metformin for 30 h and 57 h, respectively. The cells were then subjected to flow cytometric cell cycle profile analysis. The results are representative of three independent experiments
    Zr 75 1 Breast Cancer Cells, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    zr 75 1 breast cancer cells - by Bioz Stars, 2024-06
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    Cytotoxicity of metformin in HeLa and ZR-75-1 cells. a and b HeLa cells ( a ) and ZR-75-1 ( b ) cells were treated with the indicated concentration of metformin for 35 h and 70 h, respectively. Cell viability was measured using the MTT method. c HeLa and ZR-75-1 cells were incubated with indicated concentration of metformin for 20 h and 25 h, respectively. Cell lysates were subjected to western blot analysis using antibodies against cyclin D1, cyclin B1 and H3P. ACTN was the protein loading control. The protein levels of cyclin D1, cyclin B1 and H3P after normalization with the loading control protein ACTN are presented as fold change. d HeLa and ZR-75-1 cells were incubated with the indicated concentration of metformin for 30 h and 57 h, respectively. The cells were then subjected to flow cytometric cell cycle profile analysis. The results are representative of three independent experiments

    Journal: Journal of Biomedical Science

    Article Title: Metformin causes cancer cell death through downregulation of p53-dependent differentiated embryo chondrocyte 1

    doi: 10.1186/s12929-018-0478-5

    Figure Lengend Snippet: Cytotoxicity of metformin in HeLa and ZR-75-1 cells. a and b HeLa cells ( a ) and ZR-75-1 ( b ) cells were treated with the indicated concentration of metformin for 35 h and 70 h, respectively. Cell viability was measured using the MTT method. c HeLa and ZR-75-1 cells were incubated with indicated concentration of metformin for 20 h and 25 h, respectively. Cell lysates were subjected to western blot analysis using antibodies against cyclin D1, cyclin B1 and H3P. ACTN was the protein loading control. The protein levels of cyclin D1, cyclin B1 and H3P after normalization with the loading control protein ACTN are presented as fold change. d HeLa and ZR-75-1 cells were incubated with the indicated concentration of metformin for 30 h and 57 h, respectively. The cells were then subjected to flow cytometric cell cycle profile analysis. The results are representative of three independent experiments

    Article Snippet: ZR-75-1 breast cancer cells were cultivated in Roswell Park Memorial Institute (RPMI) 1640 medium supplemented with 10% FBS and 1% penicillin-streptomycin (Invitrogen).

    Techniques: Concentration Assay, Incubation, Western Blot