Fig. 2.
Fig. 2. Cell cycle analysis of purified c-kit+ Thy-1.1lo Lin−/lo Sca-1+ cells from splenectomized mice after G-CSF mobilization. Mice were splenectomized and, after 7 weeks, infused continuously for 7 days with G-CSF (250 μg/kg/d). c-kit+ Thy-1.1lo Lin−/lo Sca-1+ cells were purified and the cells were stained with Hoechst 33342 for analysis of DNA content. The FACS plots show Hoechst 33342 staining versus forward scatter of c-kit+ Thy-1.1lo Lin−/lo Sca-1+ cells isolated from the (a) BM or (b) MPB of G-CSF–treated mice. The percentage of cells in G0/G1 or S/G2/M is indicated on the left or right side of each FACS plot, respectively.

Cell cycle analysis of purified c-kit+ Thy-1.1lo Lin−/lo Sca-1+ cells from splenectomized mice after G-CSF mobilization. Mice were splenectomized and, after 7 weeks, infused continuously for 7 days with G-CSF (250 μg/kg/d). c-kit+ Thy-1.1lo Lin−/lo Sca-1+ cells were purified and the cells were stained with Hoechst 33342 for analysis of DNA content. The FACS plots show Hoechst 33342 staining versus forward scatter of c-kit+ Thy-1.1lo Lin−/lo Sca-1+ cells isolated from the (a) BM or (b) MPB of G-CSF–treated mice. The percentage of cells in G0/G1 or S/G2/M is indicated on the left or right side of each FACS plot, respectively.

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