首页 | 本学科首页   官方微博 | 高级检索  
检索        

ADAM9基因真核表达质粒的构建及表达
引用本文:乔纯忠,卞倩,戚宇华,焦永军,李俊生.ADAM9基因真核表达质粒的构建及表达[J].东南大学学报(医学版),2011,30(3):482-485.
作者姓名:乔纯忠  卞倩  戚宇华  焦永军  李俊生
作者单位:1. 东南大学,医学院,江苏,南京,210009
2. 江苏省疾病预防控制中心,病原微生物研究所,江苏,南京,210009
基金项目:江苏省自然科学基金资助项目
摘    要:目的:构建人源性去整合素金属蛋白酶9(ADAM9)基因真核表达载体并表达其编码蛋白(转染293T细胞).方法:利用包含ADAM9全长编码核酸序列的质粒PCR4-TOPO作为模板,用PCR扩增其核心编码区,将其克隆至PMD18-T Vector中构建PMD18-T-ADAM9质粒,同时双酶切PMD18-T-ADAM9及P...

关 键 词:去整合素金属蛋白酶9  真核表达载体  293T  免疫印记

Construction and eukaryotic expression of ADAM9 gene
QIAO Chun-zhong,BIAN Qian,QI Yu-hua,JIAO Yong-jun,LI Jun-sheng.Construction and eukaryotic expression of ADAM9 gene[J].Journal of Southeast Univ: Medical Sci Ed,2011,30(3):482-485.
Authors:QIAO Chun-zhong  BIAN Qian  QI Yu-hua  JIAO Yong-jun  LI Jun-sheng
Institution:QIAO Chun-zhong1,BIAN Qian2,QI Yu-hua2,JIAO Yong-jun2,LI Jun-sheng1(1.Medical School,Southeast University,Nanjing 210009,China,2.Institute of Pathogenic Microbiology,Jiangsu Provincial Center for Disease Prevention and Control,China)
Abstract:Objective: To construct human a disintegrin and metalloprotease 9(ADAM9) gene into a eukaryotic expression vector PXJ40-HA and study the expression of ADAM9 gene in transfected 293T cells.Methods: ADAM9 gene was amplified from a vector PCR4-TOPO ordered from Open Biosystems and cloned into PMD18-T vector to construct a vector named PMD18-T-ADAM9.The PMD18-T-ADAM9 and the PXJ40-HA double digested by the same restrict enzymes,the recombinant eukaryotic expression vector PXJ40-HA-ADAM9 subsequently yielded.The...
Keywords:293T
本文献已被 CNKI 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