Creating random mutagenesis libraries using megaprimer PCR of whole plasmid

The conventional method for cloning a DNA fragment is to insert it into a vector and ligate it. Although this method is commonly used, it is labor intensive because the ratio and concentrations of the DNA insert and the vector need optimizing. Even then, the resultant library is often plagued with u...

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Bibliographische Detailangaben
Veröffentlicht in:BioTechniques. - 1993. - 33(2002), 5 vom: 21. Nov., Seite 1033-4, 1036-8
1. Verfasser: Miyazaki, Kentaro (VerfasserIn)
Weitere Verfasser: Takenouchi, Misa
Format: Aufsatz
Sprache:English
Veröffentlicht: 2002
Zugriff auf das übergeordnete Werk:BioTechniques
Schlagworte:Evaluation Study Journal Article DNA Primers DNA, Recombinant Luminescent Proteins Green Fluorescent Proteins 147336-22-9 Pfu DNA polymerase EC 2.7.7.- Taq Polymerase mehr... DNA-Directed DNA Polymerase EC 2.7.7.7