| Literature DB >> 6086459 |
J Davison, M Heusterspreute, M Merchez, F Brunel.
Abstract
A DNA fragment has been constructed that contains many unique cloning sites not present in currently used Escherichia coli plasmid cloning vehicles. Insertion of this fragment into a modified version of pBR322 results in an AmpRTetR vector (pJRD158) of 3903 bp containing 28 unique cloning sites, four "almost unique" cloning sites, and eight unassigned unique 6-bp palindromes. The plasmid has the additional advantages of very high copy number and altered incompatibility. The latter permits it to be stably maintained in the same host as pBR322.Entities:
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Year: 1984 PMID: 6086459 DOI: 10.1016/0378-1119(84)90148-3
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688