A general method for rapid site-directed mutagenesis using the polymerase chain reaction
- 29 January 1990
- Vol. 96 (1) , 125-128
- https://doi.org/10.1016/0378-1119(90)90351-q
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Rapid insertional mutagenesis of DNA by polymerase chain reaction (PCR)Nucleic Acids Research, 1989
- A general method of site-specific mutagenesis using a modification of the Thermus aquaticus polymerase chain reactionAnalytical Biochemistry, 1989
- Site-directed mutagenesis by overlap extension using the polymerase chain reactionGene, 1989
- Use of polymerase chain reaction catalyzed by Taq DNA polymerase for site-specific mutagenesisGene, 1989
- Precise gene fusion by PCRNucleic Acids Research, 1989
- Expression of Ribonuclease T1 in Escherichia Coli and Rapid Purification of the EnzymeNucleosides and Nucleotides, 1988
- KGB: a single buffer for all restriction endonucleasesNucleic Acids Research, 1988
- Novel non-templated nucleotide addition reactions catalyzed by procaryotic and eucaryotic DNA polymerasesNucleic Acids Research, 1988
- Supercoil Sequencing: A Fast and Simple Method for Sequencing Plasmid DNADNA, 1985
- Analysis of restriction fragments of T7 DNA and determination of molecular weights by electrophoresis in neutral and alkaline gelsJournal of Molecular Biology, 1977