Creating Random Mutagenesis Libraries by Megaprimer PCR of Whole Plasmid (MEGAWHOP)

AbstractThe conventional method for cloning a DNA fragment is to insert it into a vector and ligate it (1). Although this method is commonly used, it is labor intensive because the ratio and concentrations of the DNA insert and the vector must be optimized. Even then, the resulting library is often plagued with unwanted plasmids that have no inserts or multiple inserts. These species have to be eradicated to avoid tedious screening, especially when producing random mutagenesis libraries.KeywordsExonuclease ActivityTemplate PlasmidSpecific Restriction EnzymeSingle InsertMultiple InsertThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.