In vitro mutagenesis protocols /
| Other Authors: | |
|---|---|
| Format: | Book |
| Language: | English |
| Published: |
Totowa, N.J. :
Humana Press,
[1996]
|
| Series: | Methods in molecular biology (Clifton, N.J.) ;
v. 57. |
| Subjects: |
Table of Contents:
- Site-directed mutagenesis using positive antibiotic selection
- In vitro site-directed mutagenesis using the unique restriction site elimination (USE) method
- Site-directed mutagenesis using double-stranded plasmid DNA templates
- Site-directed mutagenesis using a uracil-containing phagemid template
- Oligonucleotide-directed mutagenesis using an improved phosphorothioate approach
- Analysis of point mutations by use of amber stop codon suppression
- A simple method for site-directed mutagenesis with double-stranded plasmid DNA
- Double-stranded DNA site-directed mutagenesis
- Solid-phase in vitro mutagenesis using a plasmid DNA template
- Targeted mutagenesis mediated by the triple helix formation
- A universal nested deletion method using an arbitrary primer and elimination of a unique restriction site
- Ordered deletions using exonuclease III
- Ligase chain reaction for site-directed in vitro mutagenesis
- PCR-based site-directed mutagenesis
- In vitro recombination and mutagenesis by overlap extension PCR
- Site-directed mutagenesis using overlap extension PCR
- Modification of the overlap extension method for extensive mutagenesis on the same template
- Site-directed mutagenesis in vitro by megaprimer PCR
- Using PCR for rapid site-specific mutagenesis in large plasmids
- PCR-assisted mutagenesis for site-directed insertion/deletion of large DNA segments
- Site-directed mutagenesis using a rapid PCR-based method
- A simple method to introduce internal deletions or mutations into any position of a target DNA sequence
- A simple method for site-specific mutagenesis that leaves the rest of the template unaltered
- Multiple site-directed mutagenesis
- Construction of linker-scanning mutations by oligonucleotide ligation
- Construction of linker-scanning mutations using PCR
- Use of codon cassette mutagenesis for saturation mutagenesis
- Saturation mutagenesis by mutagenic oligonucleotide-directed PCR amplification (mod-PCR)
- Random mutagenesis of short target DNA sequences via PCR with degenerate oligonucleotides
- Random sequence mutagenesis for the generation of active enzymes
- Random mutagenesis by using mixtures of dNTP and dITP in PCR
- PCR-mediated chemical mutagenesis
- Oligonucleotide-directed random mutagenesis using the phosphorothioate method
- An efficient random mutagenesis technique using an E. coli mutator strain