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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

刘永光 刘克锋 孙向阳

安徽农业科学2011,Vol.39Issue(21):12707-12709,3.
安徽农业科学2011,Vol.39Issue(21):12707-12709,3.

RT-PCR克隆广谱抗病基因NPR1及其蛋白表达载体构建

Cloning of Broad-spectrum Anti-disease Gene NPR1 with RT-PCR and Construction of Its Protein Expression Vector

刘永光 1刘克锋 2孙向阳2

作者信息

  • 1. 北京林业大学水保学院,北京100083
  • 2. 北京农学院城乡发展学院,北京102206
  • 折叠

摘要

Abstract

[Objective] It is to clone broad-spectrum anti-disease gene NPRl and to construct its protein expression vector. [Method] First extract Arabidopsis thaliana total RNA and design relevant primers, and then the method of reverse transcription PCR is adopted. With the method of enzyme ligation, this gene will be directed into protein expression vector. [ Result] After relevant testing, NPRl will be inserted into vector pMXBlO to obtain pMXBlO-NPRl protein expression vector. [Conclusion] Protein expression vector with NPRl will be successfully constructed.

关键词

NPR1/广谱抗病/栽体构建

Key words

Nonexpressor of pathogenesis-related genes 1/ Broad-spectrum anti-disease/ Construction of vectors

分类

农业科技

引用本文复制引用

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].安徽农业科学,2011,39(21):12707-12709,3.

基金项目

北京市教委面上项目(KM200910020014) (KM200910020014)

北京市园林绿化局治沙办项目(2008). (2008)

安徽农业科学

0517-6611

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