Fig. 2.
Fig. 2. Dot plot display of a typical Hoechst 33342 (X axis) and Pyronin Y (Y axis) staining of fresh bone marrow CD34+ cells (A). The three sort windows R1, R2, and R3 were constructed to collect G0 , G1 , and S/G2 + M cells, respectively. After sorting, G0 , G1 , and S/G2 + M cells, along with unsorted total CD34+ cells were stained with propidium iodide and analyzed for their cell-cycle distribution as described in Materials and Methods. B depicts the cell cycle distribution of total freshly isolated BM CD34+ cells with only 11% being in S/G2 + M. C, D, and E illustrate the DNA content of sorted G0 , G1 , and S/G2 + M cells, respectively. As can be seen, no cells were detected with greater than 2n DNA among G0 and G1 cells (C and D, respectively), whereas all sorted S/G2 + M cells displayed a DNA content characteristic of their position in the cell cycle (E).

Dot plot display of a typical Hoechst 33342 (X axis) and Pyronin Y (Y axis) staining of fresh bone marrow CD34+ cells (A). The three sort windows R1, R2, and R3 were constructed to collect G0 , G1 , and S/G2 + M cells, respectively. After sorting, G0 , G1 , and S/G2 + M cells, along with unsorted total CD34+ cells were stained with propidium iodide and analyzed for their cell-cycle distribution as described in Materials and Methods. B depicts the cell cycle distribution of total freshly isolated BM CD34+ cells with only 11% being in S/G2 + M. C, D, and E illustrate the DNA content of sorted G0 , G1 , and S/G2 + M cells, respectively. As can be seen, no cells were detected with greater than 2n DNA among G0 and G1 cells (C and D, respectively), whereas all sorted S/G2 + M cells displayed a DNA content characteristic of their position in the cell cycle (E).

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