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mtt cell viability kit  (Biotium)


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    Structured Review

    Biotium mtt cell viability kit
    Mtt Cell Viability Kit, supplied by Biotium, used in various techniques. Bioz Stars score: 95/100, based on 176 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mtt cell viability kit/product/Biotium
    Average 95 stars, based on 176 article reviews
    mtt cell viability kit - by Bioz Stars, 2026-06
    95/100 stars

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    Biotium mtt solution
    Effects of HNF 14 on cellular metabolic activity in <t>AMD</t> <t>cybrids.</t> Cellular metabolic activity was assessed using an <t>MTT</t> assay in normal and age-related macular degeneration (AMD) transmitochondrial cybrid cells treated with HNF 14 (3.2 µM) for 48 h. Individual data points represent biological replicates, and horizontal bars indicate the mean ± SD ( n = 5 biological replicates). Data were normalized to untreated normal cybrids. Statistical significance is indicated as * p < 0.05, ** p < 0.01, *** p < 0.001; ns, not significant.
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    Biotium 3 4 5 dimethylthiazol 2 yl 2 5 diphenyltetrazolium
    Cell viability levels of SK‐BR‐3 and MCF‐7 determined by MTT assay. (A, B) Effects of single (A) and in combination (B) therapeutic agents on cell viability in HER2 + (SK‐BR‐3) and HER2 − (MCF‐7) breast cancer (BC) cell lines. The data is expressed as mean ± SD of three independent experiments ( N = 3). Statistical significance was determined by ANOVA followed by Dunnett's T3 post hoc test, where * p ‐value < 0.05; ** p ‐value < 0.01; *** p ‐value < 0.001 in comparison with the control group. (C) Experiments at the level of 3D cell lines, when incubated with D+T+P+N+I (Denosumab+Trastuzumab+Pertuzumab+Nivolumab+Ipilimumab) in HER2 + BC, resulted in a clinically significant reduction in cell viability, possibly through immunomodulation of the tumour microenvironment (TME), characterised by a marked increase in tumour‐infiltrating lymphocytes (TILs) infiltration and a possibly concurrent decrease in pro‐tumorigenic neutrophils (created using BioRender ( https://biorender.com/ )). ANOVA, analysis of <t>variance;</t> <t>MTT,</t> <t>3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium</t> bromide; SD, standard deviation.
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    Effects of HNF 14 on cellular metabolic activity in AMD cybrids. Cellular metabolic activity was assessed using an MTT assay in normal and age-related macular degeneration (AMD) transmitochondrial cybrid cells treated with HNF 14 (3.2 µM) for 48 h. Individual data points represent biological replicates, and horizontal bars indicate the mean ± SD ( n = 5 biological replicates). Data were normalized to untreated normal cybrids. Statistical significance is indicated as * p < 0.05, ** p < 0.01, *** p < 0.001; ns, not significant.

    Journal: Journal of Clinical Medicine

    Article Title: Characterization of the Effects of a Humanin Fragment Peptide (HNF 14 ) in Age-Related Macular Degeneration

    doi: 10.3390/jcm15051686

    Figure Lengend Snippet: Effects of HNF 14 on cellular metabolic activity in AMD cybrids. Cellular metabolic activity was assessed using an MTT assay in normal and age-related macular degeneration (AMD) transmitochondrial cybrid cells treated with HNF 14 (3.2 µM) for 48 h. Individual data points represent biological replicates, and horizontal bars indicate the mean ± SD ( n = 5 biological replicates). Data were normalized to untreated normal cybrids. Statistical significance is indicated as * p < 0.05, ** p < 0.01, *** p < 0.001; ns, not significant.

    Article Snippet: AMD and normal cybrids plated in 96-well tissue culture plates were treated with MTT solution (Catalog number: 30006, Biotium, Fremont, CA, USA) at the 48 h time point.

    Techniques: Activity Assay, MTT Assay

    Cell viability levels of SK‐BR‐3 and MCF‐7 determined by MTT assay. (A, B) Effects of single (A) and in combination (B) therapeutic agents on cell viability in HER2 + (SK‐BR‐3) and HER2 − (MCF‐7) breast cancer (BC) cell lines. The data is expressed as mean ± SD of three independent experiments ( N = 3). Statistical significance was determined by ANOVA followed by Dunnett's T3 post hoc test, where * p ‐value < 0.05; ** p ‐value < 0.01; *** p ‐value < 0.001 in comparison with the control group. (C) Experiments at the level of 3D cell lines, when incubated with D+T+P+N+I (Denosumab+Trastuzumab+Pertuzumab+Nivolumab+Ipilimumab) in HER2 + BC, resulted in a clinically significant reduction in cell viability, possibly through immunomodulation of the tumour microenvironment (TME), characterised by a marked increase in tumour‐infiltrating lymphocytes (TILs) infiltration and a possibly concurrent decrease in pro‐tumorigenic neutrophils (created using BioRender ( https://biorender.com/ )). ANOVA, analysis of variance; MTT, 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide; SD, standard deviation.

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: The Role of HER2 and RANK in Breast Cancer and New Therapeutic Approaches With Denosumab, Anti‐HER2 Antibodies and Immunotherapy

    doi: 10.1111/jcmm.71071

    Figure Lengend Snippet: Cell viability levels of SK‐BR‐3 and MCF‐7 determined by MTT assay. (A, B) Effects of single (A) and in combination (B) therapeutic agents on cell viability in HER2 + (SK‐BR‐3) and HER2 − (MCF‐7) breast cancer (BC) cell lines. The data is expressed as mean ± SD of three independent experiments ( N = 3). Statistical significance was determined by ANOVA followed by Dunnett's T3 post hoc test, where * p ‐value < 0.05; ** p ‐value < 0.01; *** p ‐value < 0.001 in comparison with the control group. (C) Experiments at the level of 3D cell lines, when incubated with D+T+P+N+I (Denosumab+Trastuzumab+Pertuzumab+Nivolumab+Ipilimumab) in HER2 + BC, resulted in a clinically significant reduction in cell viability, possibly through immunomodulation of the tumour microenvironment (TME), characterised by a marked increase in tumour‐infiltrating lymphocytes (TILs) infiltration and a possibly concurrent decrease in pro‐tumorigenic neutrophils (created using BioRender ( https://biorender.com/ )). ANOVA, analysis of variance; MTT, 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide; SD, standard deviation.

    Article Snippet: Following treatment, the reagent 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide (MTT) (30006, Biotium Inc., Landing Parkway, Fremont, CA, USA) was added to each well at a final concentration of 0.5 mg/mL.

    Techniques: MTT Assay, Comparison, Control, Incubation, Standard Deviation