Gene Cloning and Sequencing of Rotavirus VP7
Peng Wang
Abstract
Peng Wang
Abstract
The antigenic determinant of Rotavirus VP7 genes was amplified from cell infected by rotavirus by reverse transcription polymerase chain reaction(RT PCR). The lenth of target gene was 916 bp.The products of RT PCR were ligated with plasmid pGEM T and transformated to E.coli DH5α.By the analysis of restriction endonuclease and PCR ,the fragment of VP7 was cloned and the recombinant plasmid PT V7 was constructed.The result of nucleotid sequencing showed that the inserted gene had positive reading frame.
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The antigenic determinant of Rotavirus VP7 genes was amplified from cell infected by rotavirus by reverse transcription polymerase chain reaction(RT PCR). The lenth of target gene was 916 bp.The products of RT PCR were ligated with plasmid pGEM T and transformated to E.coli DH5α.By the analysis of restriction endonuclease and PCR ,the fragment of VP7 was cloned and the recombinant plasmid PT V7 was constructed.The result of nucleotid sequencing showed that the inserted gene had positive reading frame.
Key concepts: Rotavirus, Gene, Plasmid, Biology, Restriction enzyme, Cloning (programming), Open reading frame, Molecular biology