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新疆细毛羊eIF3l基因的克隆、原核表达及蛋白检测

于常江 沈敏 杨华 杨永林 祁成年 张云生

畜牧与兽医2017,Vol.49Issue(8):16-20,5.
畜牧与兽医2017,Vol.49Issue(8):16-20,5.

新疆细毛羊eIF3l基因的克隆、原核表达及蛋白检测

Cloning, prokaryoctic expression and protein measurement of the gene eIF3l in Xinjiang Fine-wool sheep

于常江 1沈敏 2杨华 2杨永林 2祁成年 2张云生1

作者信息

  • 1. 塔里木大学动物科学学院,新疆阿拉尔843300
  • 2. 绵羊遗传改良与健康养殖国家重点实验室,新疆石河子832000
  • 折叠

摘要

Abstract

In order to study the sequence characteristics,expression in E.coli BL21 (DE3) and identification of protein in vitro of eukaryotic translation initiation factor 3 L gene (eIF3l) in Xinjiang Fine-wool sheep,we cloned the CDS encoding sequence of eIF3l gene from the Xinjiang Fine-wool sheep fibroblasts by RT-PCR,and constructed the prokaryotic expression vector,induced the expression.The results showed that eIF3l gene sequences of CDS was got successfully,and the length of the CDS was 1 695 bp and coded 564 amino acids.The E.coli containing recombinant vector expressed inclusion body proteins of 69 ku after induction by 1 mmol/L IPTG.Western blotting revealed that the expressed protein was the target protein,which indicated that the recombinant prokaryotic expression vector expressed successfully.Together,our works made a foundation for the study of function and application of the eIF3l gene.

关键词

新疆细毛羊/eIF3l基因/载体构建/原核表达

Key words

Xinjiang Fine-wool sheep/eIF3l gene/vector construction/prokaryotic expression

分类

农业科技

引用本文复制引用

于常江,沈敏,杨华,杨永林,祁成年,张云生..新疆细毛羊eIF3l基因的克隆、原核表达及蛋白检测[J].畜牧与兽医,2017,49(8):16-20,5.

基金项目

国家“863”计划(2013AA102506) (2013AA102506)

国家自然科学基金项目(30960249) (30960249)

兵团种质资源创新与功能基因发掘及利用专项(2012BB044) (2012BB044)

畜牧与兽医

OA北大核心CSTPCD

0529-5130

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