Zhou Qi, Chy Hun, Laslett Andrew L
Commonwealth Scientific and Industrial Research Organization, Molecular and Health Technologies, Clayton, Australia.
Curr Protoc Stem Cell Biol. 2010 Jul;Chapter 1:Unit1B.7. doi: 10.1002/9780470151808.sc01b07s14.
This unit describes a useful approach to preparing highly reproducible samples of human embryonic stem cell (hESC) total RNA suitable for transcriptional profiling from heterogeneous mixtures of cells containing undifferentiated hESC and differentiated cell types. In this unit, fluorescence-activated cell sorting (FACS) is used to sub-fractionate hESC populations on the basis of their levels of co-expression of two previously published hESC surface markers, CD9(TG30) and GCTM-2. This sub-fractionation allows for the separation of undifferentiated hESC (CD9hi, GCTM-2hi) from the early stages in hESC differentiation (CD9neg or low, GCTM-2neg or low).
本单元介绍了一种制备高度可重复的人胚胎干细胞(hESC)总RNA样本的有用方法,该样本适用于从包含未分化hESC和分化细胞类型的异质细胞混合物中进行转录谱分析。在本单元中,荧光激活细胞分选(FACS)用于根据两种先前发表的hESC表面标志物CD9(TG30)和GCTM-2的共表达水平对hESC群体进行亚分级。这种亚分级允许从未分化的hESC(CD9高表达、GCTM-2高表达)与hESC分化早期阶段(CD9阴性或低表达、GCTM-2阴性或低表达)中分离出来。