Skip to main content
. 1998 Aug 4;95(16):9448–9453. doi: 10.1073/pnas.95.16.9448

Figure 2.

Figure 2

Defects in B-lymphopoiesis and myelopoiesis and normal T lymphopoiesis in CXCR4−/− mice determined by flow cytometry. (A and B) Pro-B cells (B220+CD43+) within lymphocyte scatter gates were enumerated in E18.5 fetal liver (A) and 5 day Whitlock–Witte culture with IL-7 of E15.5 fetal liver cells (B). (C) Staining of Gr-1+CD11b+ (Upper) and CD18+CD11b+ (Lower) myeloid cells within scatter gates for myelomonocytic cells in E18.5 fetal liver. E18.5 fetal thymocytes (D) or cells from thymic organ culture of E15.5 thymus (E) were stained with CD4 and CD8 mAb. The percentages of gated cells within the boxes are indicated.