Fig. 3.
Fig. 3. The HB-LTC CD19+ VpreB+population is composed of predominantly large, cycling cells. B-lineage cells were separated from 8-week-old HB-LTC by positive selection using anti-CD19 magnetic beads and stained with anti-VpreB and anti-IgM antibodies and analyzed by flow cytometry. (A) (Left) Forward and side scatter analysis of total cell population showing gated R1 (smallest) or R2 (largest) cell populations. (Right) VpreB+ and VpreB− populations in gates R1 or R2, with numbers indicating the percentages of the total CD19+ cell population in each quadrant. (B) Cell cycle analysis of CD19+VpreB+ cells. CD19+ were stained with the anti-VpreB antibody before permeabilization and staining with propidium iodide for FACS analysis of DNA content versus surface VpreB expression (R3 = VpreB− and R4 = VpreB+ populations, respectively). Numbers indicate the relative percentage of cells in S/G2/M.

The HB-LTC CD19+ VpreB+population is composed of predominantly large, cycling cells. B-lineage cells were separated from 8-week-old HB-LTC by positive selection using anti-CD19 magnetic beads and stained with anti-VpreB and anti-IgM antibodies and analyzed by flow cytometry. (A) (Left) Forward and side scatter analysis of total cell population showing gated R1 (smallest) or R2 (largest) cell populations. (Right) VpreB+ and VpreB populations in gates R1 or R2, with numbers indicating the percentages of the total CD19+ cell population in each quadrant. (B) Cell cycle analysis of CD19+VpreB+ cells. CD19+ were stained with the anti-VpreB antibody before permeabilization and staining with propidium iodide for FACS analysis of DNA content versus surface VpreB expression (R3 = VpreB and R4 = VpreB+ populations, respectively). Numbers indicate the relative percentage of cells in S/G2/M.

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