2002•Zhongguo yufang shouyi xuebaoRequires access

Cloning and Sequensing of NP Gene of Newcastle Disease Virus F_(48)E_9 Strain

Qingyin Wang

Open publisher page 0 citations

Abstract

According to published NP protein gene sequence of NDV.We designed and synthesized a pair of primers.A 1598bp fragment was amplified from F 48E 9 strain by means of RT-PCR and cloned into the pMD18-T vector.The recombinant plasmid was proved to be true by enzyme analysis and PCR.In order to further identify the credibility of the gene,the sequence of the cDNA was obtained by sanger′s sequencing technique.Compared the obtained gene sequence of F 48E 9 strain with the corresponding sequence of La Sota strain by DNASIS software,the homology of the nucleotide sequence was 88.2%.As a result,we obtained complete NP gene clone of NDV F 48E 9 strain.

About this research paper

What this paper is about

According to published NP protein gene sequence of NDV.We designed and synthesized a pair of primers.A 1598bp fragment was amplified from F 48E 9 strain by means of RT-PCR and cloned into the pMD18-T vector.The recombinant plasmid was proved to be true by enzyme analysis and PCR.In order to further identify the credibility of the gene,the sequence of the cDNA was obtained by sanger′s sequencing technique.Compared the obtained gene sequence of F 48E 9 strain with the corresponding sequence of La Sota strain by DNASIS software,the homology of the nucleotide sequence was 88.2%.As a result,we obtained complete NP gene clone of NDV F 48E 9 strain.

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

According to published NP protein gene sequence of NDV.We designed and synthesized a pair of primers.A 1598bp fragment was amplified from F 48E 9 strain by means of RT-PCR and cloned into the pMD18-T vector.The recombinant plasmid was proved to be true by enzyme analysis and PCR.In order to further identify the credibility of the gene,the sequence of the cDNA was obtained by sanger′s sequencing technique.Compared the obtained gene sequence of F 48E 9 strain with the corresponding sequence of La Sota strain by DNASIS software,the homology of the nucleotide sequence was 88.2%.As a result,we obtained complete NP gene clone of NDV F 48E 9 strain.

Key concepts: Biology, Gene, Homology (biology), Complementary DNA, Recombinant DNA, Molecular biology, Cloning (programming), Nucleic acid sequence

Related papers

Back to paper searchBrowse research topicsOriginal source
Cloning and Sequensing of NP Gene of Newcastle Disease Virus F_(48)E_9 Strain — Research Paper | ScholarLens