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. 2012 Jan 30;109(7):2364–2369. doi: 10.1073/pnas.1121385109

Fig. 1.

Fig. 1.

Fractionation of LincKit+Sca1IL7RαFcγRII/IIIloCD150+ bone marrow with CD9 and endoglin. (A) Flow cytometry fractionation of LincKit+Sca1IL7RαFcγRII/IIIloCD150+ bone marrow cells by endoglin and CD9 expression into CD9loendoglinlo, CD9hiendoglinlo, and CD9loendoglinhi populations. Isotype control (contour plot). (B) CD9loendoglinlo (Left), CD9hiendoglinlo (Center), and CD9loendoglinhi (Right) cytocentrifuge preparations stained with May–Grunwald–Giemsa stain. (C) Comparison of CD9loendoglinlo, CD9hiendoglinlo, and CD9loendoglinhi LincKit+Sca1IL7RαFcγRII/IIIloCD150+ bone marrow fractions with CD9hiMkP, PreCFU-E, and PreMeg-E populations (Table S1) by flow cytometry.