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RT-PCR克隆广谱抗病基因NPR1及其蛋白表达载体构建
引用本文:刘永光,刘克锋,孙向阳.RT-PCR克隆广谱抗病基因NPR1及其蛋白表达载体构建[J].农业科学与技术,2011(6):852-854,930.
作者姓名:刘永光  刘克锋  孙向阳
作者单位:北京林业大学水保学院;北京农学院城乡发展学院
基金项目:Supported by project of Beijing Municipal Education Commission(KM200910020014);Project of Sand Control Department,Beijing Municipal Landscape Greening Bureau(2008)~~
摘    要:目的]克隆植物广谱抗病基因NPR1并构建其蛋白表达载体。方法]提取拟南芥总RNA,设计相关引物,采用反转录PCR方法克隆NPR1基因;利用酶切连接方法,将该基因正向导入蛋白表达载体。结果]经过相关检验,将NPR1正向插入pMXB10载体中,得到了pMXB10-NPR1蛋白表达载体。结论]成功构建了包含NPR1的蛋白表达载体。

关 键 词:NPR1  广谱抗病  载体构建

Cloning of Broad-spectrum Anti-disease NPR1 Gene with RT-PCR and Construction of Its Protein Expression Vector
LIU Yong-guang,LIU Ke-feng,SUN Xiang-yang.Cloning of Broad-spectrum Anti-disease NPR1 Gene with RT-PCR and Construction of Its Protein Expression Vector[J].Agricultural Science & Technology,2011(6):852-854,930.
Authors:LIU Yong-guang  LIU Ke-feng  SUN Xiang-yang
Institution:1.School of Soil and Water Conservation,Beijing Forestry University,Beijing 100083;2.College of Urban and Rural Development,Beijing University of Agriculture,Beijing 102206
Abstract:
Keywords:Nonexpressor of pathogenesis-related genes 1(NPR1)  Broad-spectrum anti-disease  Construction of vectors
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