首页> 外国专利> METHOD FOR ENHANCING PRDUCTIVITY OF HUMAN INTERFERONE BETA MONOMER THROUGH CULTURING TRANSFORMED CELL LINE AT LOW TEMPERATURE AND HYPEROSMOSIS

METHOD FOR ENHANCING PRDUCTIVITY OF HUMAN INTERFERONE BETA MONOMER THROUGH CULTURING TRANSFORMED CELL LINE AT LOW TEMPERATURE AND HYPEROSMOSIS

机译:通过低温低温渗透培养的转化细胞系提高人干扰素β单体产量的方法

摘要

PURPOSE: A method for enhancing productivity of human interferon beta monomer by reducing aggregation of the human interferon beta is provided.;CONSTITUTION: A productivity of human interferon beta monomer is enhanced by transforming the cell line for expressing human interferon beta and culturing in a medium of hyperosmosis. The cell line is CHO(Chinese hamster ovary), VERO, BHK, HeLa, Cv1, MDCK, 293, 3T3, myeloma, PC12 or WI38 cell. The used cell line is CHO cell in which DHFR gene is deleted. The condition of hyperosmosis is 350~550 mOsm/kg. The medium is serum-free medium. A method for enhancing producitivity of human interferone beta monomer comprises a step of transferring transformed cell line to medium of hyperosmosis to express human interferon beta.;COPYRIGHT KIPO 2010
机译:目的:提供一种通过减少人干扰素β的聚集来提高人干扰素β单体生产率的方法。;组成:通过转化表达人干扰素β的细胞系并在培养基中培养,可以提高人干扰素β单体的生产率。高渗。细胞系是CHO(中国仓鼠卵巢),VERO,BHK,HeLa,Cv1,MDCK,293、3T3,骨髓瘤,PC12或WI38细胞。使用的细胞系是其中DHFR基因缺失的CHO细胞。高渗条件为350〜550 mOsm / kg。培养基是无血清培养基。一种提高人干扰素β单体生产率的方法,包括将转化细胞系转移到高渗培养基中以表达人干扰素β的步骤。COPYRIGHTKIPO 2010

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