摘要
为了克隆抗肿瘤因子内皮抑素基因并表达内皮抑素蛋白,从人胎盘组织中分离总RNA, 用RT PCR 法扩增出570 bp 的DNA 片段,并成功地克隆到pUC18 质粒载体中,经序列测定证实为内皮抑素基因,用Xpress 系统体外表达出内皮抑素蛋白并纯化成功.
To clone and express human endostatin, total RNA was isolated from human placenta tissue and endostatin gene was amplified by RT PCR. Then, the 570 bp endostatin gene fragment was cloned into pUC18 vector for sequencing. It was expressed and purified by Xpress system. The success of cloning and expression of human endostatin gene will provide tool for high level expression of it and further clinical application as antitumor drug.
出处
《扬州大学学报(自然科学版)》
CAS
CSCD
1999年第4期35-37,共3页
Journal of Yangzhou University:Natural Science Edition
基金
国家卫生部科学基金