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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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Bibliografiske detaljer
Udgivet i:Nucleic Acids Res
Principais autores: Chen, X, Liu, W, Quinto, I, Scala, G
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 1997
Fag:
Online adgang: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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