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Construction,prokaryotic expression and purification of FimH1-156 fusion protein / 重庆医学
Chongqing Medicine ; (36): 589-591, 2014.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-443808
Responsible library: WPRO
ABSTRACT
Objective To construct and express a prokaryotic expression vector carrying the gene of FimH 1-156 that comprises human lysosome membrane protein 2 P41-49 gene ,and to express and purify the fusion protein .Methods FimH1-156 gene was cloned from plasmid pPKL241 by PCR ,and inserted into vector pET-28a(+ ) to obtain prokaryotic expression plasmid pET-28a-FimH . After transforming Escherichia coli BL21(DE3) with pET-28a-FimH ,fusion protein FimH1-156 was expressed under induction .The target fusion protein was purified ,and its antigenicity was detected through Western blot .Results The expressed recombinant pro-tein was purified ,the expression of protein was the highest when IPTG was 1 mmol/L and 4h after induction ,it was expressed as include body form ,and the expressed protein was identified to react with monoclonal antibodies 6 × His by Western blotting .Conclu-sion We cloned FimH1-156 fusion protein expressed genes successfully ,constructed prokaryotic expression vector ,and won the in-clusion body purification of FimH1-156 fusion protein .

Full text: Available Database: WPRIM (Western Pacific) Language: Chinese Journal: Chongqing Medicine Year: 2014 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Language: Chinese Journal: Chongqing Medicine Year: 2014 Document type: Article
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