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- W2359790735 abstract "According to the Genbank open sequence,one pair of primers was designed in order to amply VP_2 of porcine parvovirus NADL-2,and StuⅠ site was introduced on the upper stream and SphⅠ site on the lower stream of the primers.The VP_2 gene was obtained by polymerase chain reaction(PCR) and subsequently was cloned into pGEM-T vector,producing the recombinant plasmid pVP_2.A recombinant plasmid pPR128,composed of the gI,gE,11K,gD genes and partial sequences of gG,28K genes of Pseudorabies virus(PRV)Min-A,was eliminated partial gI and gE genes by StuⅠ and SphⅠ digestion,then was inserted by VP_2 gene and finally produced the pPR-VP_2 vector." @default.
- W2359790735 created "2016-06-24" @default.
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- W2359790735 date "2006-01-01" @default.
- W2359790735 modified "2023-09-26" @default.
- W2359790735 title "Construction of the Pseudorabies Virus Transfer Vector to Express Porcine Parvovirus VP_2 Gene" @default.
- W2359790735 hasPublicationYear "2006" @default.
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