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Expression and Purification of the DNA Binding Domain of the Epstein-Barr Virus Nuclear Antigen 1
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作者 Meiru Hu~1 Ru Wei~(1,2)Lu Qian~1 Ming Yu~1 Ming Shi~1 Kun He~3 Jie Wang~3 Beifen Shen~1 Ning Guo~1 (1 Institute of Basic Medical Sciences,beijing 100850 2 North China Coal Medical College 3 national center of biomedical analysis,beijing 100071) 《生物技术通报》 CAS CSCD 2008年第S1期405-410,共6页
To overexpress EBNA-1 in E.coli and generate the specific antibody,in this study,the antigenicity,epitope and hydrolysis of EBNA-1 were analyzed using the computer design software Biosun.Based on the prediction by com... To overexpress EBNA-1 in E.coli and generate the specific antibody,in this study,the antigenicity,epitope and hydrolysis of EBNA-1 were analyzed using the computer design software Biosun.Based on the prediction by computer analysis,the sequence encoding EBNA-1385-557 was amplified by PCR with the specific primers.The expression vector containing EBNA-1385-557 coding sequence was constructed.His-tagged EBNA-1385-557 was expressed in E.coli.The soluble recombinant protein was purified using Ni-NTA chromatography.The purified protein was used as antigens to immunize mice and screen the antibodies,which will serve as an important tool for further studies. 展开更多
关键词 EBNA-1 EXPRESSION PURIFICATION E.COLI
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