The Construction of Recombinant Plasmid Containing gE Gene Epitope Encoding Area of Pseudorabies Virus Fa Strain
AO Jingqun
Abstract
AO Jingqun
Abstract
The gE gene epitope encoding area of pseudorabies virus Fa strain was amplified by PCR from template plasmid pMD18T_FS.Then the PCR products were cloned into pPICZaA and pAcGP67A vector respectively.The recombinant plasmids pPICZaA_FS and pAcGP67A_FS were identified by double restriction endonuclease digestion and DNA sequence analysis.The sequencing results showed that the recombinant plasmid contained the gE gene epitope encoding area of PRV Fa strain.
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The gE gene epitope encoding area of pseudorabies virus Fa strain was amplified by PCR from template plasmid pMD18T_FS.Then the PCR products were cloned into pPICZaA and pAcGP67A vector respectively.The recombinant plasmids pPICZaA_FS and pAcGP67A_FS were identified by double restriction endonuclease digestion and DNA sequence analysis.The sequencing results showed that the recombinant plasmid contained the gE gene epitope encoding area of PRV Fa strain.
Key concepts: Pseudorabies, Recombinant DNA, Restriction enzyme, Plasmid, Biology, Epitope, Virology, Gene