High efficiency of site-directed mutagenesis mediated by a single PCR product.

We describe a highly efficient procedure for site-specific mutagenesis of double-stranded plasmids. The method relies on a single PCR primer which incorporates both the mutations at the selection site and the desired single base substitutions at the mutant site. This primer is annealed to the denatu...

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Veröffentlicht in:	Nucleic Acids Res
Hauptverfasser:	Chen, X, Liu, W, Quinto, I, Scala, G
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Oxford University Press 1997
Schlagworte:	Research Article
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC146466/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9016615/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/25.3.682
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