| Literature DB >> 8200531 |
S Mongkolsuk1, S Rabibhadana, P Vattanaviboon, S Loprasert.
Abstract
We have modified the positive-selection cloning vector pUN121 to expand the numbers of unique cloning sites by insertion of a multiple cloning site into the lambda cI gene without disrupting its repressor function, resulting in plasmid pSKM10. Plasmid pSKM10 has seven restriction enzyme sites suitable for general cloning purposes. A mobilizable version (pSKM11) of pSKM10 was constructed by insertion of the IncP mob sequence which permitted mobilization of the plasmid into a wide variety of Gram- bacteria.Entities:
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Year: 1994 PMID: 8200531 DOI: 10.1016/0378-1119(94)90620-3
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688