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人IgG1FccDNA的克隆与鉴定
引用本文:安云庆,柯岩,陈金栋.人IgG1FccDNA的克隆与鉴定[J].首都医学院学报,2000,21(2):93-96.
作者姓名:安云庆  柯岩  陈金栋
作者单位:首都医科大学微生物学和免疫学教研室
基金项目:国家自然科学基金资助项目 !(395 70 6 6 6 )
摘    要:根据编码人IgG1Fc(Fcγ1 )的基因序列 ,设计合成 1对与之相匹配的引物。采用RT PCR法 ,从正常人白细胞mRNA中扩增获得预期目的基因Fcγ1 70 0bp基因片段 ,成功构建PUC1 8 Fcγ1 70 0 重组克隆载体 ,酶切、酶谱分析与预期结果相符 ;DNA测序结果与GenBank报道一致。

关 键 词:I_gG1Fc(Fcγ1)  PUC18-Fcγ1_(700)重组克隆载体  RT-PCR
收稿时间:1999-08-27

Cloning and Identification of Human IgG1Fc cDNA
An Yunqing,Ke Yan,Chen Jindong.Cloning and Identification of Human IgG1Fc cDNA[J].Journal of Capital University of Medical Sciences,2000,21(2):93-96.
Authors:An Yunqing  Ke Yan  Chen Jindong
Institution:Department of Microbiology and Immunology, Capital University of Medical Sciences
Abstract:According to the cDNA sequences which encode the human IgG1Fc, a pair of primers were designed; The expected gene (Fcγ1700bp) which encode Fcγ1 was amplified by RT-PCR from mRNA extracted from normal person′s leukocyte; PUC18-Fcγ1700 recombinant cloning vector was successfully constructed, and the enzyme digestion analysis are identical to expected results. Sequences are identical to those in GenBank report.
Keywords:RT-PCR
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