首页 | 本学科首页   官方微博 | 高级检索  
检索        

人血管内皮细胞生长因子165基因真核表达载体构建
引用本文:吴波,陈秉,熊群英,容振勤,张伟林,李永浩.人血管内皮细胞生长因子165基因真核表达载体构建[J].医学研究杂志,2006,35(1):16-17.
作者姓名:吴波  陈秉  熊群英  容振勤  张伟林  李永浩
作者单位:1. 广东省江门中医药学校,529000
2. 广东药学院
3. 中山大学眼科医院
摘    要:目的获得人血管内皮生长因子(hVEGF165)cDNA,构建其真核表达载体。方法采用PCR技术,从HL60细胞中扩增出hVEGF165 cDNA,将其克隆至pcDNA3真核表达载体上,构建成为pCD-hVGEF165重组质粒。结果经酶切鉴定,克隆的基因片段为人hVGEF165 cDNA;建立了pCD-hVGEF165重组质粒。结论成功地克隆和表达出了人VEGF165基因,为大量制备重组质粒的研究奠定了基础。

关 键 词:血管内皮生长因子  克隆  基因表达
收稿时间:2005-08-22
修稿时间:2005年8月22日

Construction of Eukaryotic Expression Vector Containing Human Vascular Endothelial Growth Factor 165 Gene
Wu Bo,Chen Bing,Xiong Qunying.Construction of Eukaryotic Expression Vector Containing Human Vascular Endothelial Growth Factor 165 Gene[J].Journal of Medical Research,2006,35(1):16-17.
Authors:Wu Bo  Chen Bing  Xiong Qunying
Institution:Jiangmeng School of Traditional Chinese Medicine and Pharmacology, Jiangmeng 529000, China
Abstract:Objective To clone human vascular endothelial growth factor 165(hVEGF_ 165 ),construct its eukaryotic expression and to study the expression of hVEGF_ 165 . Methods Human vascular endothelial growth factor cDNA was amplified by PCR method from the HL60 cells and cloned to expression vector pcDNA_3,constructed pCD-hVGEF_ 165 recombinant plasmid, then transformed to E.coli BL21(DE3)cell.Results The cloned cDNA was confirmed to be VGEF_ 165 cDNA. It was observed that the expression of human VEGF gene was detected distinctly 72h after transferring.Conclusions We successfully cloned and expressed hGEF_ 165 gene, which provided the further foundation of the model of VEGF transgenic animal and makes a basis for the further study in retinal neovascularization.
Keywords:Vascular endothelial growth factor  Clone  Gene expression
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《医学研究杂志》浏览原始摘要信息
点击此处可从《医学研究杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号