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人表皮生长因子真核表达载体的构建
引用本文:赵国强,张立华,王莉,鲍玉洲. 人表皮生长因子真核表达载体的构建[J]. 郑州大学学报(医学版), 2004, 39(4): 603-605
作者姓名:赵国强  张立华  王莉  鲍玉洲
作者单位:郑州大学基础医学院微生物学与免疫学教研室,郑州,450052;河南省人民医院,河南省眼科研究所分子生物室,郑州,450003
基金项目:河南省科研事业发展计划项目  0 14 1163 2 16
摘    要:目的:构建人表皮生长因子的真核表达载体。方法:采用RT-PCR扩增人表皮生长因子(hEGF)cDNA基因序列并克隆入PGEM-T载体,再用限制性内切酶切取目的基因,插入pcDNA3.1真核表达载体。结果:重组体经转化E.coli JM109感受态大肠杆菌后可大量扩增,提取重组体进行限制性酶切及PCR可见目的片段。结论:已成功构建hEGF真核表达载体,为进一步研究hEGF的功能奠定了基础。

关 键 词:人表皮生长因子  克隆  基因表达
修稿时间:2003-09-04

Construction of eukaryotic expression vector for human epidermal growth factor
ZHAO Guoqiang ),ZHANG Lihua ),WANG Li ),BAO Yuzhou ) ). Construction of eukaryotic expression vector for human epidermal growth factor[J]. Journal of Zhengzhou University: Med Sci, 2004, 39(4): 603-605
Authors:ZHAO Guoqiang )  ZHANG Lihua )  WANG Li )  BAO Yuzhou ) )
Affiliation:ZHAO Guoqiang 1),ZHANG Lihua 2),WANG Li 2),BAO Yuzhou 2) 1)Department of Microbiology & Immunology,College of Basic Medical Sciences,Zhengzhou University,Zhengzhou 450052 2)Laboratory of Molecular Biology,Henan Provincial Hospital,Henan Institute of Ophthalmology,Zhengzhou 450003
Abstract:Aim: To construct eukaryotic expression vector of human epidermal growth factor. Methods: The cDNA sequence of human epidermal growth factor was amplified by RT PCR and then cloned into PGEM T Easy vector. After the sequence was analyzed, it was cut by restriction endonuclease and subcloned into eukaryotic expression vector pcDNA3.1. Results: The target fragment could be found when recombination had transformed into the competent cell E.coli JM109, then was cut by restriction endonuclease and identified by PCR. Conclusion: The eukaryotic expression vector of human epidermal growth factor has been successfully constructed and it could lay the foundation for future research.
Keywords:human epidermal growth factor  clone  gene expression
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