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口蹄疫病毒RNA复制酶基因3D的克隆、表达及纯化
引用本文:孙涛,陆苹.口蹄疫病毒RNA复制酶基因3D的克隆、表达及纯化[J].中国兽医学报,2005,25(2):119-121.
作者姓名:孙涛  陆苹
作者单位:上海交通大学,农业生物技术学院,生物技术研究所,上海,201101
摘    要:利用RT-PCR扩增了口蹄疫病毒(FMDV)的RNA复制酶基因,并将其克隆到原核表达载体pET-32a( )中。重组质粒在大肠杆菌中表达后的目的蛋白为可溶性形式,纯化产物用感染A型FMDV的豚鼠康复血清进行Western-blotting检测,结果表明,3D基因得到了正确的表达。

关 键 词:口蹄疫病毒  RNA复制酶基因  基因表达  基因克隆  基因纯化
文章编号:1005-4545(2005)02-0119-03
修稿时间:2003年11月3日

Cloning,Expression and Purification of Replicase Gene of Foot-and-Mouth Disease Virus
SUN Tao,LU Ping.Cloning,Expression and Purification of Replicase Gene of Foot-and-Mouth Disease Virus[J].Chinese Journal of Veterinary Science,2005,25(2):119-121.
Authors:SUN Tao  LU Ping
Abstract:The RNA replicase gene of foot-and-mouth virus was amplified and cloned into prokaryotic expression vector pET-32a(+).The recombinant plasmid was transformed into E.coli and the target protein was expressed in soluble form.The purified recombinant protein was substantiated to be expressed correctly by Western-blotting.
Keywords:foot-and-mouth virus  RNA replicase gene  expression
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