Figure 1
Figure 1. Isolation of LSK/EPCR+ cells using flow cytometric and CFU-C analysis. (A) After mature blood cell lineage predepletion, E12.5 mouse FL cells were gated against viable immature hematopoietic cells. Subsequently, the LSK fraction was determined and was subdivided into EPCR+ and EPCR− fractions. Sorted LSK/EPCR+ and LSK/EPCR− cells were submitted to CFU-C analysis. LSK/EPCR+ cells formed a significantly higher number of colonies at all observation stages (B), as well as a larger variety of colonies (C). Error bars represent SD (n = 3). *P < .05, **P < .01.

Isolation of LSK/EPCR+ cells using flow cytometric and CFU-C analysis. (A) After mature blood cell lineage predepletion, E12.5 mouse FL cells were gated against viable immature hematopoietic cells. Subsequently, the LSK fraction was determined and was subdivided into EPCR+ and EPCR fractions. Sorted LSK/EPCR+ and LSK/EPCR cells were submitted to CFU-C analysis. LSK/EPCR+ cells formed a significantly higher number of colonies at all observation stages (B), as well as a larger variety of colonies (C). Error bars represent SD (n = 3). *P < .05, **P < .01.

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