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- W2355887609 abstract "The total RNA was isolated from the purified merozoite of ovine Theileria.The major surface protein P32 gene was amplified by RT-PCR and then cloned into pGEM-T Easy vector. Positive clones were identified by PCR screening and EcoRⅠ digestion and sequenced.To construct recombinant eukaryotic expression vector, the P32 gene was cleaved from the pGEM-T Easy plasmids by double restriction endonuclease digestion, and then subcloned into the Pichia pastoris expression vector pPIC9K,and the recombinant plasmid pPIC9K-MPSP-P32 was transformed into E.coli JM109. The gene sequencing suggested that the result was correct." @default.
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- W2355887609 date "2009-01-01" @default.
- W2355887609 modified "2023-09-25" @default.
- W2355887609 title "Cloning of the Major Surface Protein P32 Gene from Ovine Theileria and Construction of Eukaryotic Expression Vector" @default.
- W2355887609 hasPublicationYear "2009" @default.
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