In vitro mutagenesis protocols /

Bibliographic Details
Other Authors: Trower, Michael K.
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