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人hTERT基因的pCIneo真核表达载体的构建Q78
引用本文:滕勇,李旭升,关玉成,李雁军.人hTERT基因的pCIneo真核表达载体的构建Q78[J].西北国防医学杂志,2011,32(5):335-337.
作者姓名:滕勇  李旭升  关玉成  李雁军
作者单位:1. 兰州军区乌鲁木齐总医院全军骨科中心骨一科,新疆乌鲁木齐,830000
2. 解放军68202部队医院
基金项目:兰州军区医药卫生科研计划资助项目(LXH2007014)
摘    要:构建人端粒酶逆转录酶(hTERT)片段的基因的pCIneo真核表达载体。方法:根据hTERTmRNA序列设计引物,人胚肾转化细胞系293总RNA反转录得到的cDNA为模板,PCR扩增后克隆到载体pCIneo上,并进行酶切鉴定及测序。结果-酶切结果表明hTERT基因已经插入pCIneo真核表达载体,测序结果显示,核苷酸序列的同源性为99.89%,氨基酸序列的同源性为100%。结论:成功构建hTERT基因的pCIneo真核表达载体,为其下一步的研究奠定了基础。

关 键 词:人端粒酶逆转录酶  表达载体  基因转染

Construction of pCIneo eukaryotic expression plasmid of hTERT
TENG Yong,LI Xu-sheng,GUAN Yu-cheng,et al..Construction of pCIneo eukaryotic expression plasmid of hTERT[J].Medical Journal of National Defending Forces in Northwest China,2011,32(5):335-337.
Authors:TENG Yong  LI Xu-sheng  GUAN Yu-cheng  
Institution:TENG Yong,LI Xu-sheng,GUAN Yu-cheng,et al.(Department of Orthopedics,Urumqi General Hospital of Lanzhou Command,PLA,Urumqi 830000,China)
Abstract:Objective:To construct pCIneo eukaryotic expression plasmid of hTERT.Methods: The primers were designed according to hTERT mRNA sequence and the hTERT gene was amplified by RT-PCR using 293 cells as template.Then gene of hTERT was subcloned into vectors pCIneo and confirmed by DNA sequence analysis and restriction endonuclease digestion.Results: The analysis result of recombinant vector by restriction endonuclease digestion showed that hTERT gene has been correctly inserted into plasmid pCIneo.The homology ...
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