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鸡p15INK4B基因的克隆表达及纯化
引用本文:艾永兴,张玉静,胡薇,郝军元,邹亚学,张英波.鸡p15INK4B基因的克隆表达及纯化[J].吉林农业大学学报,2006,28(4):453-457,461.
作者姓名:艾永兴  张玉静  胡薇  郝军元  邹亚学  张英波
作者单位:1. 吉林大学畜牧兽医学院,长春,130062
2. 吉林农业大学生物技术学院,长春,130118
摘    要:为研究鸡p15INK4B蛋白的功能及为制备此蛋白的单克隆抗体提供材料,应用引物搭桥法合成p15INK4B基因,应用基因工程的手段构建p15INK4B基因的原核表达载体,在E.coliRosetta(DE3)菌进行融合表达,并对表达产物进行亲和层析纯化。结果成功地构建了p15INK4B基因原核表达载体,经亲和层析制备了较高纯度的目的表达产物。

关 键 词:p15INK4B  细胞周期  原核表达  亲和层析
文章编号:1000-5684(2006)04-0453-05
收稿时间:2005-12-27
修稿时间:2005-12-272006-04-20

Clone Expression and Purification of p15INK4B Gene of Chicken
Ai Yong-xing,ZHANG Yu-jing,HU Wei,HAO Jun-yuan,ZOU Ya-xue,ZHANG Ying-bo.Clone Expression and Purification of p15INK4B Gene of Chicken[J].Journal of Jilin Agricultural University,2006,28(4):453-457,461.
Authors:Ai Yong-xing  ZHANG Yu-jing  HU Wei  HAO Jun-yuan  ZOU Ya-xue  ZHANG Ying-bo
Institution:1. College of Animal Husbandry and Veterinary Medicine, Jilin University, Changchun 130062, China ; 2. College of Biotechnology , Jilin Agricultural University, Changchun 130118, China
Abstract:To study p15~(INK4B) protein and prepare its monoclonal antibody,p15~(INK4B) gene was obtained by overlap-ligation PCR and cloned into expression vector.Then p15~(INK4B) gene was expressed in E.coli Rosetta(DE3) and p15~(INK4B) fusion protein was purified by affinity chromatography.The results indicated that the recombinant expression vector pET28a( )-p15 was successfully constructed and relatively pure target protein was obtained.
Keywords:p15~(INK4B)  cell cycle  prokaryotic expression  affinity chromatography  
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