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Cloning, expression and identification of IL-1ra-Fcepsilon fusion gene / 生物工程学报
Chinese Journal of Biotechnology ; (12): 1754-1760, 2008.
Article ي Zh | WPRIM | ID: wpr-275344
المكتبة المسؤولة: WPRO
ABSTRACT
Both interleukin-1 and IgE are important in the pathogenic mechanism of the allergy asthma. cDNA of interleukin-1receptor antagonist (IL-1ra) and IgE were cloned and a prokaryotic expression vector IL-1ra-Fcepsilon/pBV220 was constructed. The vector was transformed into Escherichia coli BL21(DE3). The fusion protein was expressed successfully in the form of inclusion body. The recombination protein of IL-1ra-Fcepsilon was highly purified by chromatography of gel filtration and ion exchange, which was identifited by Western blotting. The cell assay showed that the activity of IL-1ra-Fcepsilon was as high as IL-1ra in vitro after refolding. The pharmacokenetic profile of IL-1ra-Fcepsilon and L-1ra was analyzed, and the half time of IL-1ra-Fcepsilon is 4.78 times than that of IL-1ra.
الموضوعات
النص الكامل: 1 الفهرس: WPRIM الموضوع الرئيسي: Recombinant Fusion Proteins / Immunoglobulin E / Immunoglobulin Fc Fragments / Cloning, Molecular / Escherichia coli / Gene Fusion / Interleukin 1 Receptor Antagonist Protein / Genetics / Metabolism اللغة: Zh مجلة: Chinese Journal of Biotechnology السنة: 2008 نوع: Article
النص الكامل: 1 الفهرس: WPRIM الموضوع الرئيسي: Recombinant Fusion Proteins / Immunoglobulin E / Immunoglobulin Fc Fragments / Cloning, Molecular / Escherichia coli / Gene Fusion / Interleukin 1 Receptor Antagonist Protein / Genetics / Metabolism اللغة: Zh مجلة: Chinese Journal of Biotechnology السنة: 2008 نوع: Article