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从妊娠人胎盘绒毛组织克隆HLA-G1 cDNA
引用本文:韩军艳,黄亚非,吴雄文,龚非力. 从妊娠人胎盘绒毛组织克隆HLA-G1 cDNA[J]. 华中科技大学学报(医学版), 2001, 30(3): 190-192
作者姓名:韩军艳  黄亚非  吴雄文  龚非力
作者单位:华中科技大学同济医学院基础医学院免疫学教研室,
基金项目:国家自然科学基金重点课题资助项目(No.965001037)、湖北省自然科学基金资助项目(No.98J107)
摘    要:为系统研究HLA-G1分子的生物学功能,采用RT-PCR技术,从人流的胎盘绒毛组织中提取总RNA,经过逆转录合成HLA-G1的全长cDNA,插入到真核表达载体pcDNA3中,构建重组表达质粒pcDNA3-HLA-G1;转化大肠杆菌DH5α,筛选其阳性克隆株,经酶切、PCR及测序鉴定,证实HLA-G1分子的重组真核表达载体已构建成功。

关 键 词:HLA-G1  克隆
修稿时间:2000-11-14

Cloning of HLA-G1 cDNA from the First Trimester Placental Tissue
Han Junyan,Huang Yafei,Wu Xiongwen et al. Cloning of HLA-G1 cDNA from the First Trimester Placental Tissue[J]. Journal of Huazhong University of Science and Technology(Health Sciences), 2001, 30(3): 190-192
Authors:Han Junyan  Huang Yafei  Wu Xiongwen et al
Affiliation:Han Junyan,Huang Yafei,Wu Xiongwen et al Department of Immunology,School of Basic Medical Sciences,Tongji Medical College,Huazhong University of Science and Technology,Wuhan 430030
Abstract:In order to systematically study the function of HLA-G1 molecule,total RNA was extracted from the first trimester trophoblast and the full length HLA G1 cDNA was prepared by using the technique of RT-PCR. Recombinant of HLA-G1 cDNA and plasmid pcDNA3 was constructed,and then transformed into E. coli DH5α. The recombinant was confirmed by restriction enzyme analysis and PCR analysis. The result of DNA sequencing showed that the pcDNA3-HLA-G1 recombinants had successfully been constructed.
Keywords:HLA-G1  molecule cloning
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