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xtt-based cell proliferation assay kit  (Millipore)


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    Millipore xtt-based cell proliferation assay kit
    U87 and U118 glioblastoma <t>cell</t> <t>viability.</t> Notes: Cell viability was determined using the <t>XTT</t> assay. Cells were exposed to diamond nanoparticles (ND), graphite nanoparticles (NG), and graphene oxide (nGO) at concentrations of 10, 20, 50, 100, and 200 μg/mL for 24 h. Values are expressed as mean ± standard deviation (n=4, each experiment in duplicate). Statistical significance between control (C) and the treated cells is indicated by an asterisk (multifactor analysis of variance [ANOVA]; P <0.05). There was statistical significance between U87 and U118 viability ( P =0.0000) and the interaction between cell line and the type of nanoparticle ( P =0.0000).
    Xtt Based Cell Proliferation Assay Kit, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/xtt-based+cell+proliferation+assay+kit/xtt+cell+proliferation+assay/pmc05634373-63-6-11
    Average 90 stars, based on 1 article reviews
    xtt-based cell proliferation assay kit - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "Diamond, graphite, and graphene oxide nanoparticles decrease migration and invasiveness in glioblastoma cell lines by impairing extracellular adhesion"

    Article Title: Diamond, graphite, and graphene oxide nanoparticles decrease migration and invasiveness in glioblastoma cell lines by impairing extracellular adhesion

    Journal: International Journal of Nanomedicine

    doi: 10.2147/IJN.S146193

    U87 and U118 glioblastoma cell viability. Notes: Cell viability was determined using the XTT assay. Cells were exposed to diamond nanoparticles (ND), graphite nanoparticles (NG), and graphene oxide (nGO) at concentrations of 10, 20, 50, 100, and 200 μg/mL for 24 h. Values are expressed as mean ± standard deviation (n=4, each experiment in duplicate). Statistical significance between control (C) and the treated cells is indicated by an asterisk (multifactor analysis of variance [ANOVA]; P <0.05). There was statistical significance between U87 and U118 viability ( P =0.0000) and the interaction between cell line and the type of nanoparticle ( P =0.0000).
    Figure Legend Snippet: U87 and U118 glioblastoma cell viability. Notes: Cell viability was determined using the XTT assay. Cells were exposed to diamond nanoparticles (ND), graphite nanoparticles (NG), and graphene oxide (nGO) at concentrations of 10, 20, 50, 100, and 200 μg/mL for 24 h. Values are expressed as mean ± standard deviation (n=4, each experiment in duplicate). Statistical significance between control (C) and the treated cells is indicated by an asterisk (multifactor analysis of variance [ANOVA]; P <0.05). There was statistical significance between U87 and U118 viability ( P =0.0000) and the interaction between cell line and the type of nanoparticle ( P =0.0000).

    Techniques Used: XTT Assay, Standard Deviation

    Related Articles

    Proliferation Assay:

    Article Title: Diamond, graphite, and graphene oxide nanoparticles decrease migration and invasiveness in glioblastoma cell lines by impairing extracellular adhesion
    Article Snippet: Subsequently, the sections were contrasted using uranyl acetate (Sigma-Aldrich) and lead citrate (Sigma-Aldrich). cell viability using the XTT assay Cell viability was evaluated using an XTT-based cell proliferation assay kit (Sigma-Aldrich).

    Article Title: Diamond, graphite, and graphene oxide nanoparticles decrease migration and invasiveness in glioblastoma cell lines by impairing extracellular adhesion
    Article Snippet: Cell viability was evaluated using an XTT-based cell proliferation assay kit (Sigma-Aldrich).

    XTT Assay:

    Article Title: Diamond, graphite, and graphene oxide nanoparticles decrease migration and invasiveness in glioblastoma cell lines by impairing extracellular adhesion
    Article Snippet: Subsequently, the sections were contrasted using uranyl acetate (Sigma-Aldrich) and lead citrate (Sigma-Aldrich). cell viability using the XTT assay Cell viability was evaluated using an XTT-based cell proliferation assay kit (Sigma-Aldrich).

    Article Title: Diamond, graphite, and graphene oxide nanoparticles decrease migration and invasiveness in glioblastoma cell lines by impairing extracellular adhesion
    Article Snippet: Cell viability was evaluated using an XTT-based cell proliferation assay kit (Sigma-Aldrich).

    Standard Deviation:

    Article Title: Diamond, graphite, and graphene oxide nanoparticles decrease migration and invasiveness in glioblastoma cell lines by impairing extracellular adhesion
    Article Snippet: Subsequently, the sections were contrasted using uranyl acetate (Sigma-Aldrich) and lead citrate (Sigma-Aldrich). cell viability using the XTT assay Cell viability was evaluated using an XTT-based cell proliferation assay kit (Sigma-Aldrich).

    Article Title: Diamond, graphite, and graphene oxide nanoparticles decrease migration and invasiveness in glioblastoma cell lines by impairing extracellular adhesion
    Article Snippet: Cell viability was evaluated using an XTT-based cell proliferation assay kit (Sigma-Aldrich).



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    Image Search Results


    U87 and U118 glioblastoma cell viability. Notes: Cell viability was determined using the XTT assay. Cells were exposed to diamond nanoparticles (ND), graphite nanoparticles (NG), and graphene oxide (nGO) at concentrations of 10, 20, 50, 100, and 200 μg/mL for 24 h. Values are expressed as mean ± standard deviation (n=4, each experiment in duplicate). Statistical significance between control (C) and the treated cells is indicated by an asterisk (multifactor analysis of variance [ANOVA]; P <0.05). There was statistical significance between U87 and U118 viability ( P =0.0000) and the interaction between cell line and the type of nanoparticle ( P =0.0000).

    Journal: International Journal of Nanomedicine

    Article Title: Diamond, graphite, and graphene oxide nanoparticles decrease migration and invasiveness in glioblastoma cell lines by impairing extracellular adhesion

    doi: 10.2147/IJN.S146193

    Figure Lengend Snippet: U87 and U118 glioblastoma cell viability. Notes: Cell viability was determined using the XTT assay. Cells were exposed to diamond nanoparticles (ND), graphite nanoparticles (NG), and graphene oxide (nGO) at concentrations of 10, 20, 50, 100, and 200 μg/mL for 24 h. Values are expressed as mean ± standard deviation (n=4, each experiment in duplicate). Statistical significance between control (C) and the treated cells is indicated by an asterisk (multifactor analysis of variance [ANOVA]; P <0.05). There was statistical significance between U87 and U118 viability ( P =0.0000) and the interaction between cell line and the type of nanoparticle ( P =0.0000).

    Article Snippet: Cell viability was evaluated using an XTT-based cell proliferation assay kit (Sigma-Aldrich).

    Techniques: XTT Assay, Standard Deviation