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Phenotypic cell-viability assay

Typical Phenotypic Assays 10.43.1 Cell-Viability Assay... [Pg.292]

In this chapter, we describe a protocol for the systematic perturbation of patient-derived cell lines using small-molecule probes, which is both scalable to high-throughput workflow and generalizable to a variety of assays. In the protocol presented here, multiple patient-derived lymphoblastoid cell lines either mutant or wild type at a defined genetic locus (e.g., HNF4a) are perturbed by an annotated chemical library. After sufficient incubation, cells are subjected to a phenotypic assay, in this case a luminescence-based readout of cellular ATP content, that aims to quantify the effect of compounds on oxidative phosphorylation, viability, or other relevant traits. The effect of each compound is expressed as a metric that reflects the difference in compound-induced phenotypes between mutant and wild-type cells. These ratios are then... [Pg.22]


See other pages where Phenotypic cell-viability assay is mentioned: [Pg.3]    [Pg.292]    [Pg.404]    [Pg.313]    [Pg.99]    [Pg.153]    [Pg.142]    [Pg.201]    [Pg.2859]    [Pg.297]    [Pg.585]    [Pg.593]    [Pg.585]    [Pg.73]    [Pg.70]    [Pg.434]    [Pg.157]   
See also in sourсe #XX -- [ Pg.292 , Pg.293 ]




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Cell Assays

Cell viability

Cell viability assay

Phenotype

Phenotype/phenotyping

Phenotypic

Phenotypic assays

Phenotyping

Viability assays

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