
doi: 10.2144/98256st04
pmid: 9863055
A protocol combining recombination PCR and long-distance PCR is demonstrated to be highly accurate and rapid for site-directed mutagenesis of large (> 10 kb) plasmids. Application of this protocol to the generation of mutant rabies virus glycoproteins expressed by the baculovirus/insect cell system illustrates the usefulness of this approach in facilitating structure-function relationships in this important eukaryotic expression system.
Gene Expression Regulation, Viral, Recombination, Genetic, Insecta, Genes, Viral, QH301-705.5, Reverse Transcriptase Polymerase Chain Reaction, Blotting, Western, Genetic Vectors, Molecular Weight, Transformation, Genetic, Rabies virus, Mutagenesis, Site-Directed, Animals, Genetic Testing, Biology (General), Baculoviridae, Cells, Cultured, DNA Primers, Glycoproteins, Plasmids
Gene Expression Regulation, Viral, Recombination, Genetic, Insecta, Genes, Viral, QH301-705.5, Reverse Transcriptase Polymerase Chain Reaction, Blotting, Western, Genetic Vectors, Molecular Weight, Transformation, Genetic, Rabies virus, Mutagenesis, Site-Directed, Animals, Genetic Testing, Biology (General), Baculoviridae, Cells, Cultured, DNA Primers, Glycoproteins, Plasmids
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