| Literature DB >> 6285898 |
Abstract
The type II restriction endonuclease SalGI has been purified to near homogeneity. At least 80% of the protein remaining after the final stage of the preparation is SalGI restriction endonuclease; no contaminating nucleases remain detectable. The principal form of the protein under both native and denaturing conditions is a monomer of M(r) about 29000. The optimal conditions for both enzyme stability and enzyme activity have been determined.Mesh:
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Year: 1982 PMID: 6285898 PMCID: PMC1158195 DOI: 10.1042/bj2030077
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857