首页 | 本学科首页   官方微博 | 高级检索  
     检索      

大鼠肌肉素cDNA克隆及表达
引用本文:裘梁,王曼莹,唐文琴,廖志勇,张霆,陈晓丽.大鼠肌肉素cDNA克隆及表达[J].江西师范大学学报(自然科学版),2006,30(4):387-391.
作者姓名:裘梁  王曼莹  唐文琴  廖志勇  张霆  陈晓丽
作者单位:1. 江西师范大学,生命科学学院,南昌,江西,330022
2. 首都儿科研究所,北京,100020
摘    要:通过RT-PCR方法从大鼠骨骼肌中克隆到肌肉素cDNA,构建表达载体pGEX-5X-3-musclin,并在BL21大肠杆菌中成功表达了融合蛋白GST-Musclin,且对表达条件进行了优化.在最优化的表达条件下,融合蛋白的表达量达到了14.2%.

关 键 词:肌肉素  克隆  表达
文章编号:1000-5862(2006)04-0387-05
收稿时间:2006-01-12
修稿时间:2006-01-12

Rat Musclin: Cloning and Expression in Escherichia Coli
QIU Liang,WANG Man-ying,TANG Wen-qing,LIAO Zhi-yong,ZHANG Ting,CHEN Xiao-li.Rat Musclin: Cloning and Expression in Escherichia Coli[J].Journal of Jiangxi Normal University (Natural Sciences Edition),2006,30(4):387-391.
Authors:QIU Liang  WANG Man-ying  TANG Wen-qing  LIAO Zhi-yong  ZHANG Ting  CHEN Xiao-li
Institution:1. Department of Life Science, Jiangxi Normal University, Nanchang 330027, China; 2. Paediatric Institute of Capital, Beijing 100020, China
Abstract:In this paper,musclin cDNA was cloned from skeletal muscle of rat by RT-PCR.Then the gene fragment was cloned into expression vector pGEX-5x-3,and the recombinant was transformed into E coli BL21.Induced by IPTG,the fusion protein GST-musclin,a 40 kDa protein was expressed in E coli BL21.and identified in SDS-PAGE In the optimum conditions,the expression level of fusion protein was 14.2%.
Keywords:musclin  cloning  expression
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号