2010Zhongguo fuyou baojianRequires access

Study on cloning vector of pMD18-T containing group A rotavirus VP7 gene

Wu Jing

Open publisher page 0 citations

Abstract

Objective:To construct the recombinant pMD18-T vector containing group A Rotavirus VP7 gene by RT-PCR,so as to study on cloning vector of pMD18-T containing group A rotavirus VP7 gene.Methods:Through extracting the total Group A rotavirus RNA and amplifying by RT-PCR,the VP7 gene fragment was isolated and recoveried,and trsansducted into pMD18-T.After VP7 gene was extracted from the plasmid,it was detected by 1% agarose gel electrophoresis.Results:The VP7 gene was transformed into pMD18-T.After screening by blue and white plague,the recombinant DNA (vector and the VP7 gene) was selected;And the sequence analysis results were compared with those in GeneBank.Conclusion:The VP7 gene has been successfully transformed into pMD18-T vector,so as to lay a foundation for the further development of genetic engineering vaccine against rotavirus.

About this research paper

What this paper is about

Objective:To construct the recombinant pMD18-T vector containing group A Rotavirus VP7 gene by RT-PCR,so as to study on cloning vector of pMD18-T containing group A rotavirus VP7 gene.Methods:Through extracting the total Group A rotavirus RNA and amplifying by RT-PCR,the VP7 gene fragment was isolated and recoveried,and trsansducted into pMD18-T.After VP7 gene was extracted from the plasmid,it was detected by 1% agarose gel electrophoresis.Results:The VP7 gene was transformed into pMD18-T.After screening by blue and white plague,the recombinant DNA (vector and the VP7 gene) was selected;And the sequence analysis results were compared with those in GeneBank.Conclusion:The VP7 gene has been successfully transformed into pMD18-T vector,so as to lay a foundation for the further development of genetic engineering vaccine against rotavirus.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective:To construct the recombinant pMD18-T vector containing group A Rotavirus VP7 gene by RT-PCR,so as to study on cloning vector of pMD18-T containing group A rotavirus VP7 gene.Methods:Through extracting the total Group A rotavirus RNA and amplifying by RT-PCR,the VP7 gene fragment was isolated and recoveried,and trsansducted into pMD18-T.After VP7 gene was extracted from the plasmid,it was detected by 1% agarose gel electrophoresis.Results:The VP7 gene was transformed into pMD18-T.After screening by blue and white plague,the recombinant DNA (vector and the VP7 gene) was selected;And the sequence analysis results were compared with those in GeneBank.Conclusion:The VP7 gene has been successfully transformed into pMD18-T vector,so as to lay a foundation for the further development of genetic engineering vaccine against rotavirus.

Key concepts: Rotavirus, Recombinant DNA, Vector (molecular biology), Gene, Virology, Cloning (programming), Plasmid, Agarose gel electrophoresis

Related papers

Back to paper searchBrowse research topicsOriginal source
Study on cloning vector of pMD18-T containing group A rotavirus VP7 gene — Research Paper | ScholarLens