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- W2389389605 abstract "The PRRSV nucleoprotein gene amplified by RT-PCR was cloned into pMD18-T vector,and then subcloned into prokaryotic expression pGEX-6p-1,named the recombination plasmids pGEX-6p-N;The IPTG induction with concentration of 1 mmol/L were induced for 4 hours,then the soluble confeitus protein was obtained on the condition of 37 ℃,whose molecular weight was obout 39 kDa,which were identical with the predicted results.Western blotting assays suggest that the protein could react with the porcine polyclonal antibodies against PRRSV and proved that recombination N protein has immunological activity." @default.
- W2389389605 created "2016-06-24" @default.
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- W2389389605 date "2009-01-01" @default.
- W2389389605 modified "2023-09-25" @default.
- W2389389605 title "Cloning of Porcine Reproductive and Respiratory Syndrom virus(PRRSV) N Gene and Prokaryotic Expression" @default.
- W2389389605 hasPublicationYear "2009" @default.
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