Efficient random mutagenesis method with adjustable mutation frequency by use of PCR and dITP.
<%urltitle%>
Nucleic Acids Research.1993:21(3):777
Last update 30-Nov-1999, Rating n/a of 0 votes.
Write your comment
Please Login or Register to Post
A new PCR based method for the generation of nested deletions.
A simple and rapid method for generating a deletion by PCR.
A novel rapid method for detection of PCR products.
Site-directed, Ligase-Independent Mutagenesis (SLIM): a single-tube methodology approaching 100% eff
An efficient one-step site-directed and site-saturation mutagenesis protocol
TAMS technology for simple and efficient
Directed evolution of green fluorescent protein by a new versatile PCR strategy for site-directed an
A rapid and efficient method for site-directed mutagenesis using one-step overlap extension PCR.
High efficiency of site-directed mutagenesis mediated by a single PCR product.
Rapid and efficient site-directed mutagenesis by single-tube 'megaprimer' PCR method.