Figure 3
Figure 3. Comparison of c-kit expression on fetal liver and adult bone marrow cell populations that are highly enriched in their CRU content. (A) Representative profile of E14.5 viable, lin− fetal liver (FL) cells assessed for Sca1 and CD43 expression (left panel), further analyzed for the level of surface c-kit protein expression (right panel). (B) Representative profile of viable lin−Rho−SP adult bone marrow (BM) cells (left and middle panels) assessed for the level of surface c-kit protein expression (right panel). (C) Comparison of the geometric mean fluorescence intensity (MFI ± SEM, n = 2) of surface c-kit protein expression in the lin−Sca1+CD43+ fetal liver cells (shown in panel A) and lin−Rho−SP adult bone marrow cells (shown in panel B). (D) Comparison of the average fold-change (± SEM, n = 3) in c-kit gene expression relative to Gapdh between the lin−Sca1+CD43+ fetal liver cells (shown in panel A) and lin−Rho−SP adult bone marrow cells (shown in panel B).

Comparison of c-kit expression on fetal liver and adult bone marrow cell populations that are highly enriched in their CRU content. (A) Representative profile of E14.5 viable, lin fetal liver (FL) cells assessed for Sca1 and CD43 expression (left panel), further analyzed for the level of surface c-kit protein expression (right panel). (B) Representative profile of viable linRhoSP adult bone marrow (BM) cells (left and middle panels) assessed for the level of surface c-kit protein expression (right panel). (C) Comparison of the geometric mean fluorescence intensity (MFI ± SEM, n = 2) of surface c-kit protein expression in the linSca1+CD43+ fetal liver cells (shown in panel A) and linRhoSP adult bone marrow cells (shown in panel B). (D) Comparison of the average fold-change (± SEM, n = 3) in c-kit gene expression relative to Gapdh between the linSca1+CD43+ fetal liver cells (shown in panel A) and linRhoSP adult bone marrow cells (shown in panel B).

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