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FXR1真核表达载体的构建及鉴定
引用本文:杨阳,马云,符向辉,何淑雅.FXR1真核表达载体的构建及鉴定[J].南华大学学报(医学版),2010,38(1):27-30.
作者姓名:杨阳  马云  符向辉  何淑雅
作者单位:南华大学,生物化学与分子生物学教研室,湖南,衡阳,421001
基金项目:湖南省自然科学基金(07JJ3030);;湖南省卫生厅(B2006-099)资助项目
摘    要:目的构建携带人脆性X相关基因1(FXR1)的真核表达载体pCMV-HA,为研究FXR1P互作蛋白奠定基础。方法以pYESTrp3-FXR1为模板进行聚合酶链反应(PCR)特异扩增FXR1基因片断,将扩增片段经EcoR I和XhoI双酶切后克隆到pCMV-HA载体,酶切鉴定阳性克隆并测序鉴定。结果成功构建了pC-MV-HA/FXR1真核表达载体。结论pCMV-HA/FXR1真核表达载体的构建为进一步在细胞内鉴定FXR1互作蛋白奠定了基础,从而对研究FXR1在脆性X综合征中的作用机理具有深远意义。

关 键 词:脆性X综合征  FXR1基因  免疫共沉淀  

Construction and Identification of Eukaryotic Expression Vector of FXR1
YANG Yang,MA Yun,FU Xiang-hui,et al.Construction and Identification of Eukaryotic Expression Vector of FXR1[J].Journal of Nanhua University(Medical Edition),2010,38(1):27-30.
Authors:YANG Yang  MA Yun  FU Xiang-hui  
Institution:Biochemistry and Molecular Biology Department;University of South China;Hengyang;Hunan 421001;China
Abstract:Objective To clone human fragile-X-related gene 1(FXR1)and construct its eukaryotic expression vector in order to study the interactive protein with FXR1P. Methods The FXR1 gene was amplified from pYESTrp3/FXR1 plasmid,digested with EcoRI and XhoI and then cloned into eukaryotic expression vector pCMV-HA.The recombinant plasmid of pCMV-HA/FXR1 was verified by enzyme digestion and sequence analysis. Results The construction of eukaryotic expression vector pCMV-HA/FXR1 was successful and the resulted sequence...
Keywords:fragile X syndrome  FXR1 gene  Co-immunoprecipitation  
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