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 two primers...
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| Опубліковано в:: | Nucleic Acids Res |
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| Автори: | , , , |
| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Oxford University Press
1983
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| Онлайн доступ: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC326240/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6308572/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/11.15.5103 |
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