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人钠/碘同向转运体基因cDNA的克隆与序列测定
引用本文:陈立波,朱瑞森,黄梅,黄芳,费俭,郭礼和.人钠/碘同向转运体基因cDNA的克隆与序列测定[J].生物技术通讯,2003,14(6):506-508.
作者姓名:陈立波  朱瑞森  黄梅  黄芳  费俭  郭礼和
作者单位:1. 上海交通大学,附属第六人民医院,上海,200233
2. 中国科学院,生物化学与细胞生物学研究所,上海,200031
摘    要:为研究人钠/碘同向转运体(hNIS)的生物学性能和用于肿瘤放射性碘治疗的可能性,运用反转录聚合酶链反应(RT—PCR)从人甲状腺组织总RNA中扩增出hNIS基因cDNA序列,将其克隆至pUCm-T载体中。序列分析证实克隆片段与献报道的hNIS基因cDNA序列完全一致,说明已成功克隆到hNIS基因cDNA。

关 键 词:人钠/碘同向转运体基因  cDNA  克隆  序列测定
文章编号:1009-0002(2003)06-0506-03
修稿时间:2003年4月28日

Cloning and sequencing of human sodium/iodide symporter
CHEN Li-bo,ZHU Rui-sen,HUANG Mei,HUANG Fang,FEI Jian,GUO Li-he.Cloning and sequencing of human sodium/iodide symporter[J].Letters in Biotechnology,2003,14(6):506-508.
Authors:CHEN Li-bo  ZHU Rui-sen  HUANG Mei  HUANG Fang  FEI Jian  GUO Li-he
Abstract:For studying biological actions and potential utility as a radioiodide treatment for undifferentiated thyroid carcinoma and nonthyroid carcinoma, human sodium/iodide symporter (hNIS) gene cDNA was amplified with total RNA from human thyroid tissue by RT-PCR. The recombinant plasmid pUCm-T-NIS was constructed by inserting the hNIS cDNA into cloning vector pUCm-T and transformed into E.coli XL-B. Screen the positive clone which contains the cDNA of hNIS. The cloned hNIS cDNA sequence is identical to published sequence.
Keywords:human sodium/iodide symporter  cDNA cloning  sequencing  
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