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HGFK1基因真核表达载体的构建及鉴定研究
引用本文:朱昱,顾玲玲,朱敏,张法标,方哲平.HGFK1基因真核表达载体的构建及鉴定研究[J].浙江医学,2016,38(16):1329-1332,1344.
作者姓名:朱昱  顾玲玲  朱敏  张法标  方哲平
作者单位:浙江省台州医院肝胆外科
基金项目:浙江省医药卫生科技计划项目;浙江省科技计划项目
摘    要:目的构建携带人HGFK1基因的真核表达载体pcDNA3.1(-)-HGFK1。方法通过PCR方法从已经构建好的病毒穿梭载体中扩增出HGFK1基因,构建pcDNA3.1(-)-HGFK1真核表达载体,经PCR、酶切、测序、蛋白表达等方法进行鉴定。结果PCR、酶切、测序以及蛋白表达证实pcDNA3.1(-)-HGFK1载体序列正确。结论本研究成功构建了pcDNA3.1(-)-HGFK1真核表达载体,可为后续进行肝癌细胞的生物学研究提供帮助。

关 键 词:基因  HGFK1  载体构建

Construction and identification of pcDNA3.1(-)-HGFK1 plasmid
ZHU Yu,GU Lingling,ZhU Min,ZHANG Fanbiao and FANG Zheping.Construction and identification of pcDNA3.1(-)-HGFK1 plasmid[J].Zhejiang Medical Journal,2016,38(16):1329-1332,1344.
Authors:ZHU Yu  GU Lingling  ZhU Min  ZHANG Fanbiao and FANG Zheping
Institution:Taizhou Hospital of Zhejiang Province
Abstract:Objective To construct human pcDNA3.1(-)-HGFK1 gene eukaryotic expression vector. Methods HGFK1 gene was amplified by PCR method from the constructed virus shuttle vector, and the pcDNA3.1 (-) -HGFK1 eukaryotic expression vector was constructed and identified by PCR, enzyme digestion, sequencing and protein expression. Results Enzyme digestion, PCR, sequencing and protein expression showed the successful construction of pcDNA3.1 (-)-HGFK1 eukaryotic expression vector. Conclusion We construct pcDNA3.1(-)-HGFK1 eukaryotic expression vector successfully, which may be used for further study of hepatocellular carcinoma gene therapy.
Keywords:Gene  HGFK1  Vector Construction
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