首页 | 本学科首页   官方微博 | 高级检索  
     

膜联蛋白V真核表达载体的构建
引用本文:黄瑞滨,洪梅,仲任,宋善俊. 膜联蛋白V真核表达载体的构建[J]. 广西医科大学学报, 2004, 21(2): 171-173
作者姓名:黄瑞滨  洪梅  仲任  宋善俊
作者单位:华中科技大学同济医学院附属协和医院血液病学研究所,武汉,430022;华中科技大学同济医学院附属协和医院血液病学研究所,武汉,430022;华中科技大学同济医学院附属协和医院血液病学研究所,武汉,430022;华中科技大学同济医学院附属协和医院血液病学研究所,武汉,430022
基金项目:国家自然科学基金 ( No:3 0 2 0 0 10 9)
摘    要:目的:构建人膜联蛋白V基因真核表达载体,探讨人膜联蛋白V的生理功能。方法:PCR方法扩增含EcoRI及BamHI酶切位点的膜联蛋白V基因序列,对真核表达载体pcDNA3.1(-)和膜联蛋白V基因扩增产物进行双酶切,用连接酶将二者连接并转化到大肠杆菌BL21,重组质粒经测序鉴定,称为pcDNA3.1(-)AxV。结果:酶切琼脂糖电泳分析pcDNA3.1(-)AxV中含有膜联蛋白V基因,序列分析表明与文献报道的序列完全一致。结论:成功地构建了人膜联蛋白V基因的真核表达载体,为研究其生理作用奠定了基础。

关 键 词:膜联蛋白V  基因  真核表达载体
修稿时间:2004-01-10

CONSTRUCTION OF EUKARYOTIC EXPRESSION VECTOR CONTAINING HUMAN ANNEXIN V GENE
Huang Ruibin,Hong Mei,Zhong Ren,et al.. CONSTRUCTION OF EUKARYOTIC EXPRESSION VECTOR CONTAINING HUMAN ANNEXIN V GENE[J]. Journal of Guangxi Medical University, 2004, 21(2): 171-173
Authors:Huang Ruibin  Hong Mei  Zhong Ren  et al.
Abstract:Objective:To construct eukaryotic expression plasmid of human annexin V gene for further study.Methods:Annexin V gene containing EcoRI and BamHI endoenzyme site was obtained by using PCR.Double enzyme digestion was conducted for pcDNA3 1(-) and PCR product of annexin V gene.Both fragements were connected by using ligase and transferred to BL21.Reconstituted plasmid was examined by auto sequenceing assay and was namedas pcDNA3.1(-)AxV.Result:The pcDNA3 1(-)AxV plasmid was confirmed to contain correct nucleotide sequence for human annexin V gene by restriction endonuclease digestion and sequence analysis.Conclusion:A eukaryotic expression plasmid containing human annexin V gene was successfully constructed and was helpful for the research for the function of annexin V.
Keywords:annexin V  gene  eukaryotic expression plasmid
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