首页 | 本学科首页   官方微博 | 高级检索  
     检索      

BmNPV DNA解旋酶基因酵母双杂交诱饵载体的构建
引用本文:杨金宏,王代钢,卢从德,孔卫青.BmNPV DNA解旋酶基因酵母双杂交诱饵载体的构建[J].山东农业大学学报(自然科学版),2010,41(2).
作者姓名:杨金宏  王代钢  卢从德  孔卫青
作者单位:安康学院,陕西省蚕桑重点实验室,陕西,安康,725000
基金项目:陕西科技厅农业攻关项目,安康学院基金 
摘    要:为了筛选家蚕对BmNPV DNA解旋酶的受体基因,根据GenBank公布的BmNPV (T3株)的序列,设计引物对其DNA解旋酶基因的核心结构域进行PCR扩增,成功克隆该基因并利用双酶切亚克隆至酵母双杂交诱饵载体PGBKT7.实验证明重组诱饵载体不能自激活,可以作为诱饵进行蛋白结合试验.

关 键 词:家蚕核型多角体病毒  DNA解旋酶  诱饵载体  自激活

CONSTRUCTION OF YEAST TWO HYBRID SYSTEM BAIT VECTOR WITH DNA HELICASE OF BMNPV
YANG Jin-hong,WANG Dai-gang,LU Cong-de,KONG Wei-qing.CONSTRUCTION OF YEAST TWO HYBRID SYSTEM BAIT VECTOR WITH DNA HELICASE OF BMNPV[J].Journal of Shandong Agricultural University,2010,41(2).
Authors:YANG Jin-hong  WANG Dai-gang  LU Cong-de  KONG Wei-qing
Institution:YANG Jin-hong,WANG Dai-gang,LU Cong-de,KONG Wei-qing*(Ankang University,Key Sericultural Laboratory of Shaanxi,Ankang 725000,China)
Abstract:In object to screening the receptor gene of silkworm to BmNPV,basing on the genebank Nucleotides sequence of BmNPV(T3 strain),PCR was performed to amplify the sequence of DNA helicase core domain,and successfully cloned this gene,then sub-cloned this gene into yeast two hybrid bait vector pGBKT7.pGBKT7-hel was successfully recombined and had no self-activation,and can be used in yeast two hybrid as bait vector.
Keywords:BmNPV  DNA helicase  bait vector  self-activation  
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号