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Efficient site-directed mutagenesis by simultaneous use of two primers.

A rapid and efficient procedure for site specific mutagenesis is described. A double primed synthesis with a 17-mer mismatch primer and a "universal" 15-mer M13 sequencing primer was used to introduce a T to A transversion into an ompF signal peptide gene cloned in the M13mp8 vector. The t...

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Autors principals: Norris, K, Norris, F, Christiansen, L, Fiil, N
Format: Artigo
Idioma:Inglês
Publicat: 1983
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC326240/
https://ncbi.nlm.nih.gov/pubmed/6308572
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