| Literature DB >> 9016579 |
K R Oldenburg1, K T Vo, S Michaelis, C Paddon.
Abstract
We have extended the technique of PCR-directed recombination in Saccharomyces cerevisiae to develop a simple method for plasmid or gene construction in the absence of suitable restriction sites. The DNA to be cloned is PCR-amplified with 30-40 bp of homology to a linearized yeast plasmid. Co-transformation into yeast results in homologous recombination at a position directed by the PCR oligonucleotides.Entities:
Mesh:
Substances:
Year: 1997 PMID: 9016579 PMCID: PMC146432 DOI: 10.1093/nar/25.2.451
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 16.971