Figure 1.
Figure 1. Expression of Abcg2 in MEL cells before and after induction with DMSO and in primary erythroblasts during differentiation. (A) Noninduced MEL cells and MEL cells induced with 2% DMSO for 4 days were analyzed for Abcg2 mRNA by Northern blot, glyceraldehyde phosphate dehydrogenase (GAPDH)probe served as loading control. (B) Flow cytometry analysis of MEL cells after staining with anti-Abcg2 antibody Bxp-53. (C) Hoechst 33342 fluorescence in cells analyzed by flow cytometry. Shaded area in B and C indicates noninduced MEL cells; solid line in B and C, MEL cells induced with DMSO. (D) Murine splenic proerythroblasts were cultured for differentiation; samples were taken at different time points and measured for Abcg2 mRNA using microarray. Baso indicates basophilic erythroblasts; poly, polychromatic erythroblasts; and ortho, orthochromatic erythroblasts.

Expression of Abcg2 in MEL cells before and after induction with DMSO and in primary erythroblasts during differentiation. (A) Noninduced MEL cells and MEL cells induced with 2% DMSO for 4 days were analyzed for Abcg2 mRNA by Northern blot, glyceraldehyde phosphate dehydrogenase (GAPDH)probe served as loading control. (B) Flow cytometry analysis of MEL cells after staining with anti-Abcg2 antibody Bxp-53. (C) Hoechst 33342 fluorescence in cells analyzed by flow cytometry. Shaded area in B and C indicates noninduced MEL cells; solid line in B and C, MEL cells induced with DMSO. (D) Murine splenic proerythroblasts were cultured for differentiation; samples were taken at different time points and measured for Abcg2 mRNA using microarray. Baso indicates basophilic erythroblasts; poly, polychromatic erythroblasts; and ortho, orthochromatic erythroblasts.

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