AbstractA new modification of the oligonucleotide-mediated mutagenesis technique has been developed. The proposed methodology has been used to produce specific base changes in the double-stranded plasmid DNA. For this purpose, special cloning vectors have been constructed using the synthetic oligodeoxyribonucleotides. The developed method allows the production of mutant DNA from those of the wild-type with a yield of 10–20%
The advent of high-fidelity DNA polymerases that can be used to linearize and amplify whole plasmids...
AbstractA new approach to induce directed mutations in genes of study through simple cotransfection ...
A simple method that allows the rapid preparation of oligo dG-tailed plasmid vectors is presented. T...
AbstractA new modification of the oligonucleotide-mediated mutagenesis technique has been developed....
A number of reliable techniques for site directed mutagenesis have been developed (Smith, 1985), aim...
AbstractA new site-directed method for introducing mutations into any region of plasmid vector close...
Site-directed mutagenesis is an invaluable tool for functional studies and genetic engineering. Howe...
Site-specific mutagenesis was accomplished using a solid support to generate single stranded vector ...
A rapid method for constructing new cloning vectors was described. The special features taken for mu...
A new technique for conducting site-directed mutagenesis was developed. This method allows the colou...
A new efficient in vitro mutagenesis method for the generation of complete random mutant libraries, ...
Existing methods for site-directed plasmid mutagenesis are restrained by the small spectrum of modif...
Schematic of the mutagenesis protocol. PCR is carried out as described and a single-stranded nicked ...
active DNA molecules employs random chemical modification of individual base residues. More re-centl...
AbstractWe describe a simplified method for the in vitro synthesis of mutated RNA molecules. The met...
The advent of high-fidelity DNA polymerases that can be used to linearize and amplify whole plasmids...
AbstractA new approach to induce directed mutations in genes of study through simple cotransfection ...
A simple method that allows the rapid preparation of oligo dG-tailed plasmid vectors is presented. T...
AbstractA new modification of the oligonucleotide-mediated mutagenesis technique has been developed....
A number of reliable techniques for site directed mutagenesis have been developed (Smith, 1985), aim...
AbstractA new site-directed method for introducing mutations into any region of plasmid vector close...
Site-directed mutagenesis is an invaluable tool for functional studies and genetic engineering. Howe...
Site-specific mutagenesis was accomplished using a solid support to generate single stranded vector ...
A rapid method for constructing new cloning vectors was described. The special features taken for mu...
A new technique for conducting site-directed mutagenesis was developed. This method allows the colou...
A new efficient in vitro mutagenesis method for the generation of complete random mutant libraries, ...
Existing methods for site-directed plasmid mutagenesis are restrained by the small spectrum of modif...
Schematic of the mutagenesis protocol. PCR is carried out as described and a single-stranded nicked ...
active DNA molecules employs random chemical modification of individual base residues. More re-centl...
AbstractWe describe a simplified method for the in vitro synthesis of mutated RNA molecules. The met...
The advent of high-fidelity DNA polymerases that can be used to linearize and amplify whole plasmids...
AbstractA new approach to induce directed mutations in genes of study through simple cotransfection ...
A simple method that allows the rapid preparation of oligo dG-tailed plasmid vectors is presented. T...