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水稻SDG711蛋白C末端原核表达及多克隆抗体制备

张志刚 李超 林欣欣 巫光宏 杜平州 王玉琪

安徽农业科学2013,Vol.41Issue(4):1435-1437,3.
安徽农业科学2013,Vol.41Issue(4):1435-1437,3.

水稻SDG711蛋白C末端原核表达及多克隆抗体制备

Prokaryotic Expression and Polyclonal Antibody Preparation of SDG711 C-terminal from Rice

张志刚 1李超 2林欣欣 3巫光宏 3杜平州 3王玉琪3

作者信息

  • 1. 华南农业大学生命科学学院,广东广州510642
  • 2. 广东省农业生物蛋白质功能与调控重点实验室,广东广州510642
  • 折叠

摘要

Abstract

[Objective] This study aimed to conduct prokaryotic expression of rice SDG711 C-terminal and prepare its polyclonal antibody. [ Method] C-terminal of rice SDG711 containing relatively intensive antigen determinants was selected for prokaryotic expression, prokaryotic expression vector pET28a-711C was constructed and the recombinant plasmid was transformed into Escherkhia coli BL21 (DE3) competent cells. The recombinant fusion protein was induced by IPTG and purified to immunize a New Zealand white rabbit as the antigen, and polyclonal antibody was obtained for Western-blot analysis. [Result] The polyclonal antibody prepared could efficiently detect the antigen expression. [Conclusion] This study laid the foundation for further investigating the functions of SDG711 protein.

关键词

水稻/SDG723/原核表达/多克隆抗体

Key words

Rice/ SDG711/ Prokaryotic expression/ Polyclonal antibody

分类

农业科技

引用本文复制引用

张志刚,李超,林欣欣,巫光宏,杜平州,王玉琪..水稻SDG711蛋白C末端原核表达及多克隆抗体制备[J].安徽农业科学,2013,41(4):1435-1437,3.

基金项目

广东省高等学校科技创新项目(2012KJCX0021) (2012KJCX0021)

国家自然科学基金(30700052). (30700052)

安徽农业科学

0517-6611

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