Literature DB >> 12857382

A high-throughput, homogeneous microplate assay for agents that kill mammalian tissue culture cells.

Michael Pierce1, Chunwei Wang, Matt Rebentisch, Mark Endo, Mark Stump, Alexander Kamb.   

Abstract

Screens for cytostasis/cytoxicity have considerable value for the discovery of therapeutic agents and the investigation of the biology of apoptosis. For instance, genetic screens for proteins, protein fragments, peptides, RNAs, or chemicals that kill tissue culture cells may aid in identifying new cancer therapeutic targets. A microplate assay for cell death is needed to achieve throughputs sufficient to sift through thousands of agents from expression or chemical libraries. The authors describe a homogeneous assay for cell death in tissue culture cells compatible with 96- or 384-well plates. In combination with a previously described system for retroviral packaging and transduction, nearly 6000 expression library clones could be screened per week in a 96-well plate format. The screening system may also prove useful for chemical screens.

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Year:  2003        PMID: 12857382     DOI: 10.1177/1087057103008003006

Source DB:  PubMed          Journal:  J Biomol Screen        ISSN: 1087-0571


  3 in total

1.  Differential cytotoxic effects of 7-dehydrocholesterol-derived oxysterols on cultured retina-derived cells: Dependence on sterol structure, cell type, and density.

Authors:  Bruce A Pfeffer; Libin Xu; Ned A Porter; Sriganesh Ramachandra Rao; Steven J Fliesler
Journal:  Exp Eye Res       Date:  2016-02-13       Impact factor: 3.467

2.  Rapid, cell-based toxicity screen of potentially therapeutic post-transcriptional gene silencing agents.

Authors:  Tiffany A Kolniak; Jack M Sullivan
Journal:  Exp Eye Res       Date:  2011-01-21       Impact factor: 3.467

3.  Streamlined duplex live-dead microplate assay for cultured cells.

Authors:  Bruce A Pfeffer; Steven J Fliesler
Journal:  Exp Eye Res       Date:  2017-05-30       Impact factor: 3.467

  3 in total

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