Fig. 4.
Fig. 4. CXCR4, VLA-4 and VLA-5 are expressed at similar levels by cells in G0/G1 and S/G2/M. / Representative FACS histograms of intracellular CXCR4 (A), VLA-4 (B), and VLA-5 (C) staining in cultured CD34+G0/G1 (solid lines) and S/G2/M (dotted lines) CB cells. G0/G1 and S/G2/M cells were purified by Hst sorting after 5 days of culture (see legend to Figure 1) and were then stained with anti–CD34-FITC and anti–CXCR4-PE, or anti–CD34-PE and anti–VLA-4-FITC or anti–VLA-5-FITC. Solid and dotted histograms show the control data for the G0/G1 and S/G2/M cells, respectively, stained with irrelevant isotype-matched control antibodies. The S/G2/M cells showed a higher green autofluorescence than the G0/G1cells.

CXCR4, VLA-4 and VLA-5 are expressed at similar levels by cells in G0/G1 and S/G2/M.

Representative FACS histograms of intracellular CXCR4 (A), VLA-4 (B), and VLA-5 (C) staining in cultured CD34+G0/G1 (solid lines) and S/G2/M (dotted lines) CB cells. G0/G1 and S/G2/M cells were purified by Hst sorting after 5 days of culture (see legend to Figure 1) and were then stained with anti–CD34-FITC and anti–CXCR4-PE, or anti–CD34-PE and anti–VLA-4-FITC or anti–VLA-5-FITC. Solid and dotted histograms show the control data for the G0/G1 and S/G2/M cells, respectively, stained with irrelevant isotype-matched control antibodies. The S/G2/M cells showed a higher green autofluorescence than the G0/G1cells.

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