Fig. 6.
Fig. 6. Flow cytometry of peripheral blood and bone marrow of 13-week-old well-appearing Eμ-ret (Tg+) littermates and transgene-negative (Tg−) mice. (A) Density separated peripheral blood lymphocytes were stained for CD45R and IgM expression. Varying amounts of an abnormal population of CD45R+sIgM− B precursor cells are present in the Eμ-ret mice. (B) CD45R+CD43+ gated bone marrow cells from the above Eμ-ret mice along with a Tg− littermate were resolved by BP-1 and CD24 staining into the pro–B cell Fr A through C and early pre–B Fr C′. Eμ-ret mouse 2-7 was an 11-week-old with splenomegaly and adenopathy.

Flow cytometry of peripheral blood and bone marrow of 13-week-old well-appearing Eμ-ret (Tg+) littermates and transgene-negative (Tg) mice. (A) Density separated peripheral blood lymphocytes were stained for CD45R and IgM expression. Varying amounts of an abnormal population of CD45R+sIgM B precursor cells are present in the Eμ-ret mice. (B) CD45R+CD43+ gated bone marrow cells from the above Eμ-ret mice along with a Tg littermate were resolved by BP-1 and CD24 staining into the pro–B cell Fr A through C and early pre–B Fr C′. Eμ-ret mouse 2-7 was an 11-week-old with splenomegaly and adenopathy.

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