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犬新孢子虫NcSRS2基因片段的克隆及原核表达
引用本文:丁德,贾立军,其木格,薛书江,张守发.犬新孢子虫NcSRS2基因片段的克隆及原核表达[J].河南农业科学,2008(5):111-113.
作者姓名:丁德  贾立军  其木格  薛书江  张守发
作者单位:延边大学,农学院,吉林,龙井,133400
摘    要:以含有犬新孢子虫NcSRS2基因的质粒pMD18-NcSRS2为模板,应用PCR方法扩增Nc-SRS2基因,将该基因片段克隆至原核表达载体pGEX-4T-2,构建了重组表达质粒pGEX-Nc-SRS2,转化大肠杆菌BL21中并诱导表达。结果显示,克隆的基因片段长1100bp,SDS-PAGE、Western blotting分析显示,重组质粒pGEX-NcSRS2在大肠杆菌中得到了高效表达。

关 键 词:犬新孢子虫  NcSRS2基因  克隆  原核表达
文章编号:1004-3268(2008)05-0111-03
修稿时间:2008年1月16日

Cloning and Prokaryotic Expression of NcSRS2 Gene of Neospora caninum
DING De,JIA Li-jun,QI Mu-ge,XUE Shu-jiang,ZHANG Shou-fa.Cloning and Prokaryotic Expression of NcSRS2 Gene of Neospora caninum[J].Journal of Henan Agricultural Sciences,2008(5):111-113.
Authors:DING De  JIA Li-jun  QI Mu-ge  XUE Shu-jiang  ZHANG Shou-fa
Abstract:The NcSRS2 gene fragment of Neospora caninum was amplified from pMD18-NcSRS2 by PCR,and then inserte into the pGEX-4T-2 vector.The recombinant expression plasmid pGEX-NcSRS2 was successfully constructed.The gene was induced by IPTG to express in Escherichia coli BL21.Results showed that the NcSRS2 cDNA was 1100bp in length,SDS-PAGE、Western blotting analysis revealed that recombinant pGEX-NcSRS2 has been highly expressed in E.coli.
Keywords:Neospora caninum  NcSRS2 gene  Cloning  Prokaryotic expression
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