诱导多能干细胞
继代培养(生物学)
胚胎干细胞
细胞生物学
生物
干细胞
包皮
细胞培养
遗传学
植物
基因
作者
Rosita Bergström,Susanne Ström,Frida Holm,Anis Féki,Outi Hovatta
出处
期刊:Methods in molecular biology
日期:2011-01-01
卷期号:: 125-136
被引量:56
标识
DOI:10.1007/978-1-61779-201-4_9
摘要
Stem cell culture systems that rely on undefined animal-derived components introduce variability to the cultures and complicate their therapeutic use. The derivation of human embryonic stem cells and the development of methods to produce induced pluripotent stem cells combined with their potential to treat human diseases have accelerated the drive to develop xenogenic-free, chemically defined culture systems that support pluripotent self-renewal and directed differentiation. In this chapter, we describe four xeno-free culture systems that have been successful in supporting undifferentiated growth of hPSCs as well as methods for xeno-free subculture and cryopreservation of hPSCs. Each culture system consists of a xeno-free growth medium and xeno-free substratum: (1) TeSR2™ with human recombinant laminin (LN-511); (2) NutriStem™ with LN-511; (3) RegES™ with human foreskin fibroblasts (hFFs); (4) KO-SR Xeno-Free™/GF cocktail with CELLstart™ matrix.
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