Figure 3
Figure 3. RT-PCR analysis of sorted hESC-derived cell populations. (A) hESCs differentiated for 10 days were sorted for (lane 1) CD34brightCD31+Flk1+, (lane 2) CD34+CD31−Flk1+, and (lane 3) CD34−CD31−Flk1− cells and analyzed for expression of hematopoietic and endothelial transcripts. Human umbilical vein endothelial cells (H) and K562 cells (K) were used as positive controls. (B) Q-RT-PCR analysis for expression of C-MYB from sorted populations: column 1 = CD34brightCD31+Flk1+, column 2 = CD34+CD31−Flk1+, and column 3 = CD34−CD31−Flk1− cells. All samples were normalized to GAPDH expression and compared with C-MYB expression in undifferentiated hESCs. Error bars indicate plus or minus SEM; ***P < .001.

RT-PCR analysis of sorted hESC-derived cell populations. (A) hESCs differentiated for 10 days were sorted for (lane 1) CD34brightCD31+Flk1+, (lane 2) CD34+CD31Flk1+, and (lane 3) CD34CD31Flk1 cells and analyzed for expression of hematopoietic and endothelial transcripts. Human umbilical vein endothelial cells (H) and K562 cells (K) were used as positive controls. (B) Q-RT-PCR analysis for expression of C-MYB from sorted populations: column 1 = CD34brightCD31+Flk1+, column 2 = CD34+CD31Flk1+, and column 3 = CD34CD31Flk1 cells. All samples were normalized to GAPDH expression and compared with C-MYB expression in undifferentiated hESCs. Error bars indicate plus or minus SEM; ***P < .001.

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