首页 | 本学科首页   官方微博 | 高级检索  
检索        

共表达红光荧光蛋白及发夹RNA载体的构建及鉴定
引用本文:魏映辉,吴秀丽,万敏,于永利,王丽颖.共表达红光荧光蛋白及发夹RNA载体的构建及鉴定[J].吉林大学学报(医学版),2005,31(2):163-165.
作者姓名:魏映辉  吴秀丽  万敏  于永利  王丽颖
作者单位:1. 吉林大学基础医学院分子生物学教研室,吉林 长春130021;2. 吉林大学基础医学院免疫学教研室,吉林 长春130021
摘    要:目的:构建共表达红光荧光蛋白及短发夹状RNA的重组真核载体。 方法:利用亚克隆、T-A克隆和PCR技术构建pcDNA3.0/DsRed-U6-shGFR及pcDNA3.0/DsRed-U6重组载体。 结果:成功构建上述两种真核重组表达载体。 结论:这种共表达载体的构建为进一步利用RNAi技术研究真核细胞基因功能奠定了基础。

关 键 词:发光蛋白质类  质粒    
文章编号:1671-587X(2005)02-0163-03
收稿时间:2004-11-08
修稿时间:2004年11月8日

Construction and identification of vectors encoding both red fluorescent protein and shRNA
WEI Ying-hui,WU Xiu-li,WAN Min,YU Yong-Li,WANG Li-ying.Construction and identification of vectors encoding both red fluorescent protein and shRNA[J].Journal of Jilin University: Med Ed,2005,31(2):163-165.
Authors:WEI Ying-hui  WU Xiu-li  WAN Min  YU Yong-Li  WANG Li-ying
Institution:1. Department of Molecular Biology, School of Basic Medical Sciences, Jilin University, Changchun 130021, China;2. Department of Immunology, School of Basic Medical Sciences, Jilin University, Changchun 130021, China
Abstract:Objective To construct the recombinant vectors that coexpress red fluorescent protein and small hairpin RNA (shRNA). Methods The subcloning, T-A cloning, and PCR technique were used to construct the recombinant vectors,named pcDNA3.0/DsRed-U6-shGFP and pcDNA3.0/DsRed-U6. Results The recombinant expression vectors mentioned above were successfully constructed.Conclusion The successful construction of recombinant vectors can establish a feasibility to further explore the functions of specific genes in eukaryotic cells with RNAi technique
Keywords:short hairpin RNAs  luminescent proteins  plasmids
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《吉林大学学报(医学版)》浏览原始摘要信息
点击此处可从《吉林大学学报(医学版)》下载免费的PDF全文
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