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一种限制性cDNA文库的构建
引用本文:祝骥,马文丽,李凌,姚汝华,郑文岭. 一种限制性cDNA文库的构建[J]. 遗传, 2002, 24(2): 174-176
作者姓名:祝骥  马文丽  李凌  姚汝华  郑文岭
作者单位:1.华南理工大学生物工程系,广州 510641;2.第一军医大学分子生物学研究所,广州 510515;3.广州军区广州总医院分子肿瘤研究所,广州 5100101.Department of Bioengincering,South China University of Techndogy,Guangzhou 510640,China;2.Institute of Molacular Biology,First Military Medical University,Guangzhou 510515,China;3.Liu Hua Qiao Hospital,Medical Center,Guangzhou 510010,China
基金项目:国家自然科学基金 ( 39880 0 32 0 )资助
摘    要:利用本室创建的限制性显示技术RD-PCR,建立的cDNA文库,我们称之为限制性cDNA文库。该方法构建的文库因经过了限制性分组扩增,每组均含有特定的cDNA,因而大大加快了随后克隆的分离和鉴定的速度。Abstract:A kind of cDNA library constructed according to Restriction Display PCR(RD-PCR) technology setup in our lab,which was called restriction cDNA library,was introduced in this paper.In the construction of cDNA library,cDNA was digested with restriction endonuclease,linked with special adaptor,amplified with PCR in groups.Each group of the restriction cDNA library contained special cDNAs.The method greatly reduced the repetitive frequency and accelerated the speed of identification.

关 键 词:RD-PCR Key words  Restriction cDNA library  K562 cell  K562细胞  限制性cDNA文库  
文章编号:0253-9772(2002)02-0174-03
修稿时间:2001-04-24

A Method for Construction of Restriction cDNA Library
ZHU Ji ,,MA Wen-li ,LI Ling ,YAO Ru-hua ,ZHENG Wen-ling. A Method for Construction of Restriction cDNA Library[J]. Hereditas, 2002, 24(2): 174-176
Authors:ZHU Ji     MA Wen-li   LI Ling   YAO Ru-hua   ZHENG Wen-ling
Affiliation:Department of Bioengincering, South China University of Technology, Guangzhou 510640, China.
Abstract:A kind of cDNA library constructed according to Restriction Display PCR(RD-PCR) technology setup in our lab,which was called restriction cDNA library,was introduced in this paper.In the construction of cDNA library,cDNA was digested with restriction endonuclease,linked with special adaptor,amplified with PCR in groups.Each group of the restriction cDNA library contained special cDNAs.The method greatly reduced the repetitive frequency and accelerated the speed of identification.
Keywords:Restriction cDNA library  K562 cell  RD-PCR
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