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陆地棉锌指蛋白(GZFP)的原核表达
引用本文:常平安,杨召军,温镭,魏荣.陆地棉锌指蛋白(GZFP)的原核表达[J].西南农业大学学报,2007,29(3):130-133.
作者姓名:常平安  杨召军  温镭  魏荣
作者单位:重庆邮电大学生物信息学院,重庆400065
基金项目:国家自然科学基金资助项目(30440032);重庆邮电大学博士启动基金资助项目(A2005-13)
摘    要:采用大肠杆菌表达体系来获得陆地棉锌指蛋白(GZFP)的融合蛋白.以pMD18-GZFP质粒为模板,用PCR方法扩增获得GZFP基因的编码区序列,将其克隆到表达载体pET28b(+)中,转化宿主菌BL21(DE3),成功地构建了陆地棉GZFP基因原核表达载体pET—GZFP、经IPTG诱导、SDS-PAGE电泳分析和蛋白质杂交检测表明,陆地棉GZFP以融合蛋白的形式在大肠杆菌中得到大量表达.

关 键 词:锌指蛋白  原核表达  陆地棉
文章编号:1000-2642(2007)03-0130-04
修稿时间:2006-09-12

Prokaryotic Expression of A Novel Zinc Finger Protein from Upland Cotton (Gossypium hirsutum L.)
CHANG Ping-an, YANG Zhao-jun, WEN Lei, WEI Rong.Prokaryotic Expression of A Novel Zinc Finger Protein from Upland Cotton (Gossypium hirsutum L.)[J].Journal of Southwest Agricultural University,2007,29(3):130-133.
Authors:CHANG Ping-an  YANG Zhao-jun  WEN Lei  WEI Rong
Institution:College of Bio-information, Chongqing University of Posts and Telecommunications, Chongqing 400065, China
Abstract:In this study,a novel zinc finger protein(GZFP) from upland cotton(Gossypium hirsutum L.)was expressed by the E.coli expression system.The GZFP gene was amplified by PCR with pMD18-GZFP plasmid as the template,and was then cloned into the pET-28b(+) to construct pET-GZFP recombinant plasmid,which was transformed into E.coli BL21(DE3).The recombinant GZFP was induced and expressed by IPTG.SDS-PAGE analysis and Western blotting showed that the target protein was expressed at a high level in E.coli BL21(DE3).
Keywords:zinc finger protein  prokaryotic expression  Gossypiurn hirsutum L  
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