Fig. 1.
Fig. 1. Early pre-B cells are depleted in estrogen-treated BALB/c mice. / (A) B-lineage populations in bone marrow from control and E2-treated mice were revealed by surface staining with antibodies to CD45R and CD43. Mature B cells were identified as CD45RhiCD43−. (B) Cells within the CD45R+CD43+ gate were then analyzed for cμ heavy chains (solid lines) as compared with staining with a normal goat IgG control (dotted lines). The histograms depict 50 000 events collected within lymphocyte light scatter gates and are representative of results obtained from 7 individual control and 9 estrogen-treated mice.

Early pre-B cells are depleted in estrogen-treated BALB/c mice.

(A) B-lineage populations in bone marrow from control and E2-treated mice were revealed by surface staining with antibodies to CD45R and CD43. Mature B cells were identified as CD45RhiCD43. (B) Cells within the CD45R+CD43+ gate were then analyzed for cμ heavy chains (solid lines) as compared with staining with a normal goat IgG control (dotted lines). The histograms depict 50 000 events collected within lymphocyte light scatter gates and are representative of results obtained from 7 individual control and 9 estrogen-treated mice.

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