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Journal of Biomedical Engineering ; (6): 534-537, 2011.
Article in Chinese | WPRIM | ID: wpr-359230

ABSTRACT

This paper is aimed to present a research on fusion protein of human tumor necrosis factor-alpha (hTNF-alpha), matrix metalloproteinase 1 (MMP1), and foldon sequence using the methord of gene engineering. We transformed the recombinant plasmid, which contains the DNA sequences of hTNF-alpha, MMP1, and foldon sequence, into Rosetta2, and successfully induced the fusion protein to express under given conditions by isopropyl beta-D-1-Thiogalactopyranoside (IPTG). Then we purified the expression product through a glutathione S-transferase (GST) resin and collected the interested protein. This research may lay the groundwork for scientific research and clinical application.


Subject(s)
Humans , Base Sequence , Escherichia coli , Genetics , Metabolism , Matrix Metalloproteinase 1 , Genetics , Molecular Sequence Data , Recombinant Fusion Proteins , Genetics , Tumor Necrosis Factor-alpha , Genetics
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