(1) Department of Biochemistry and Molecular Biology, The University of Queensland, Brisbane Qld, 4072, Australia
Abstract:
Background
Site-directed mutagenesis is an efficient method to alter the structure and function of genes. Here we report a rapid and
efficient megaprimer-based polymerase chain reaction (PCR) mutagenesis strategy that by-passes any intermediate purification
of DNA between two rounds of PCR.