Fig. 1.
Fig. 1. Loss of hematopoietic cells in the bone marrow of IL-2−/− mice. (A) Antibodies reactive with surface antigens that distinguish various stages of B-cell development were used to identify pro- (S7+), pre- (BP1+), and mature (IgM+) B cells in the bone marrow of 6-week old IL-2−/− mice. (B) FITC-Gr–1 and PE-Ter–119 were used to distinguish cells of the myeloid and erythroid lineage, respectively. Stained cells were run on a flow cytometer and analyzed using CellQuest software. The level of staining obtained with isotype-matched control antibodies was used to establish quadrant settings for the dot plots and determine the frequency of cells stained with B cell, erythroid and myeloid cell-specific antibodies (numbers shown in each quadrant of dot plots in A and in histograms in B). The results shown are representative of 10 groups of mice.

Loss of hematopoietic cells in the bone marrow of IL-2−/− mice. (A) Antibodies reactive with surface antigens that distinguish various stages of B-cell development were used to identify pro- (S7+), pre- (BP1+), and mature (IgM+) B cells in the bone marrow of 6-week old IL-2−/− mice. (B) FITC-Gr–1 and PE-Ter–119 were used to distinguish cells of the myeloid and erythroid lineage, respectively. Stained cells were run on a flow cytometer and analyzed using CellQuest software. The level of staining obtained with isotype-matched control antibodies was used to establish quadrant settings for the dot plots and determine the frequency of cells stained with B cell, erythroid and myeloid cell-specific antibodies (numbers shown in each quadrant of dot plots in A and in histograms in B). The results shown are representative of 10 groups of mice.

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