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DIFFERENTIATION INDUCTION OF PRIMARY PRECURSOR ADIPOSE CELL, AND CULTURE MEDIUM FOR ITS DIFFERENTIATION

机译:原代前脂肪细胞的分化诱导及其分化培养基

摘要

PROBLEM TO BE SOLVED: To evaluate therapeutic agents for obesity, diabetes and the like in no need of consideration on the influence of serum components by inducing the differentiation of the primary precursor adipose cells to adipose cells in a nutrient medium containing insulin or the like, selenious acid or its salt, indomethacin or the like.;SOLUTION: The differentiation of a primary precursor adipose cells to the adipose cells is induced in a nutrient culture medium selected from among the Eagle basal medium (MEM), α-Eagle basal medium (αMEM), Dulbecco- modified Eagle medium (DMEM), and Ham' F-12 medium, including insulin, transferrin, dexamethasone, biotn, ascorbic acid, glucose, epidermal growth factor, or fibroblast growth factor, and selenious acid or its salts, in addition at least one selected from the group consisting of indomethacin, prostaglandin, long-chain fatty acid and thiazolidine derivative. In a preferred embodiment, ≤3 wt.% of serum is added to the nutrient culture.;COPYRIGHT: (C)2000,JPO
机译:要解决的问题:通过在包含胰岛素等的营养培养基中诱导初级前体脂肪细胞向脂肪细胞的分化来评估不需要考虑血清成分影响的肥胖,糖尿病等治疗药物,亚硒酸或其盐,吲哚美辛等;解决方案:在从Eagle基础培养基(MEM),α-Eagle基础培养基(MEM)中选择的营养培养基中诱导初级前体脂肪细胞向脂肪细胞的分化αMEM),Dulbecco修饰的Eagle培养基(DMEM)和Ham'F-12培养基,包括胰岛素,转铁蛋白,地塞米松,生物素,抗坏血酸,葡萄糖,表皮生长因子或成纤维细胞生长因子,以及亚硒酸或其盐,另外,选自吲哚美辛,前列腺素,长链脂肪酸和噻唑烷衍生物中的至少一种。在一个优选的实施方案中,将≤3重量%的血清添加到营养培养物中。版权所有:(C)2000,JPO

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