| Literature DB >> 19932072 |
Jeffrey W Brown1, C James McKnight.
Abstract
F-actin binding constants are traditionally determined by centrifugal cosedimentation with actin microfilaments, where bound protein is separated from actin with SDS-PAGE and quantitated using densitometry. Here, we demonstrate that UV quantitation of reverse-phase HPLC-separated proteins provides increased accuracy and sensitivity, can be fully automated, and allows one to perform F-actin competition assays on similar sized proteins. Copyright 2009 Elsevier Inc. All rights reserved.Entities:
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Year: 2009 PMID: 19932072 PMCID: PMC2812587 DOI: 10.1016/j.ab.2009.11.023
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365