| Literature DB >> 7012155 |
M M Cox, K McEntee, I R Lehman.
Abstract
A simple and rapid three-step procedure for the large scale purification of the recA protein of Escherichia coli is described. The method depends primarily on a single chromatographic step which is highly specific for recA protein: elution by ATP from single-stranded DNA cellulose. With this procedure, gram quantities of recA protein, greater than 99% pure, can be reproducibility prepared for biochemical and biophysical analysis.Entities:
Mesh:
Substances:
Year: 1981 PMID: 7012155
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157