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人血小板生成素(hTPO)的cDNA克隆与序列测定
引用本文:邢桂春 胡志远. 人血小板生成素(hTPO)的cDNA克隆与序列测定[J]. 高技术通讯, 1996, 6(3): 12-14
作者姓名:邢桂春 胡志远
作者单位:北京放射医学研究所
基金项目:国家自然科学基金,863计划资助
摘    要:由于人血小板生成素cDNA的阅读框架较长而且序列中无合适的酶切位点,因此,我们利用一个同义突变创造的KpnI酶切位点人为将hTPO cDNA分成N-端和C-端两个片段。首先利用反转录聚合酶链式反应从人胎肝mRNA中分别扩增出两个cDNA片段,于EcoRI,KpnI位点分别克隆入测序载体pUC19中。

关 键 词:cDNA克隆 序列分析 人血小板生成素

cDNA Cloning and Sequencing of Human Thrombopoietin
Xing Guichun,Hu Zhiyuan,Yang Xiaoming,Xie Ling,He Fuchu,Wu Chutse. cDNA Cloning and Sequencing of Human Thrombopoietin[J]. High Technology Letters, 1996, 6(3): 12-14
Authors:Xing Guichun  Hu Zhiyuan  Yang Xiaoming  Xie Ling  He Fuchu  Wu Chutse
Abstract:A Synonymous Substitution was used to set up a novel restriction enzyme site-KpnI,separating the total cDNA into two fragments,encoding N terminal and C terminal,respectively.The fragments were amplified from human fetalliver mRNA,coined into pUC 19 and sequenced.Their sequences were shown to be identical with hTPO cDNA reported.
Keywords:Human thrombopoietin  RT-PCR  cDNA cloning  Sequencing
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