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Chinese Journal of Biotechnology ; (12): 398-402, 2007.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-328016

ABSTRACT

cDNA for Insulin-like growth factor binding protein 3 was cloned and constructed a prokaryotic expression vector--pET-DsBA-IGFBP3. The construct was transformed into E. coli BL21 (DE3)plysS. The induced fusion protein (D-IGFBP3) was expressed successfully in soluble form. We obtained D-IGFBP3 the purify of which is over 95% after purification by His affinity chromatography. The product was identified by Western-blot. The cell assay showed that the obtained fusion protein can inhibit the growth of MCF-7 and bind with IGF-I in vitro.


Subject(s)
Humans , Blotting, Western , Cell Line, Tumor , Cell Proliferation , Chromatography, Affinity , Dose-Response Relationship, Drug , Electrophoresis, Polyacrylamide Gel , Enzyme-Linked Immunosorbent Assay , Escherichia coli , Genetics , Gene Expression , Insulin-Like Growth Factor Binding Protein 3 , Genetics , Metabolism , Pharmacology , Insulin-Like Growth Factor I , Metabolism , Protein Binding , Recombinant Proteins , Metabolism , Pharmacology , Solubility
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