2005Zhongguo shouyi ke-jiRequires access

Construction of recombinant adenovirus with IBDV VP2 gene

Chunhong Zhang

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Abstract

The recombinant plasmid pAdlox VP2 was obtained after the VP2 gene of infectious bursal disease virus (IBDV) cloned by RT-PCR was sub-cloned into the transfer vector pAdlox. The pAdlox VP2 was transfered into Cre8 cells together with the wild-type adenovirus ψ5 DNA to express the VP2 gene of IBDV. The result demonstrated that the recombinant adenovirus containing the IBDV VP2 gene was (constructed) successfully, and a 37 ku protein was expressed successfuly in the Cre8 cells, which was (confirmed) by Western-blotting method.

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What this paper is about

The recombinant plasmid pAdlox VP2 was obtained after the VP2 gene of infectious bursal disease virus (IBDV) cloned by RT-PCR was sub-cloned into the transfer vector pAdlox. The pAdlox VP2 was transfered into Cre8 cells together with the wild-type adenovirus ψ5 DNA to express the VP2 gene of IBDV. The result demonstrated that the recombinant adenovirus containing the IBDV VP2 gene was (constructed) successfully, and a 37 ku protein was expressed successfuly in the Cre8 cells, which was (confirmed) by Western-blotting method.

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Available abstract

The recombinant plasmid pAdlox VP2 was obtained after the VP2 gene of infectious bursal disease virus (IBDV) cloned by RT-PCR was sub-cloned into the transfer vector pAdlox. The pAdlox VP2 was transfered into Cre8 cells together with the wild-type adenovirus ψ5 DNA to express the VP2 gene of IBDV. The result demonstrated that the recombinant adenovirus containing the IBDV VP2 gene was (constructed) successfully, and a 37 ku protein was expressed successfuly in the Cre8 cells, which was (confirmed) by Western-blotting method.

Key concepts: Infectious bursal disease, Recombinant DNA, Virology, Biology, Molecular biology, Plasmid, Gene, Virus

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