Fig. 6.
Fig. 6. Defect in Slug mutant mice is intrinsic to the stem cell. / (A) Kit immunoprecipitations from BM-derived mast cells were probed for kit and reprobed for phosphotyrosine. Slug+/−, heterozygous mice; Slug−/−, homozygous mice; Slug+/+, wild-type mice. (B, C) Analysis of the hematopoietic system in normal recipient mice reconstituted with either Slug+/+ HSC or Slug−/− HSC by FACS. BM, spleen, and thymus samples were stained with monoclonal antibodies and were analyzed by flow cytometry. The hematopoietic composition of mice reconstituted with Slug−/− HSC is similar to that for Slug−/−mice. A representative analysis of the c-kit+ cells present in the BM and spleen of normal recipient mice reconstituted with either Slug+/+ HSC or Slug−/− HSC after the induction of hemolytic anemia with PHZ is shown.

Defect in Slug mutant mice is intrinsic to the stem cell.

(A) Kit immunoprecipitations from BM-derived mast cells were probed for kit and reprobed for phosphotyrosine. Slug+/−, heterozygous mice; Slug−/−, homozygous mice; Slug+/+, wild-type mice. (B, C) Analysis of the hematopoietic system in normal recipient mice reconstituted with either Slug+/+ HSC or Slug−/− HSC by FACS. BM, spleen, and thymus samples were stained with monoclonal antibodies and were analyzed by flow cytometry. The hematopoietic composition of mice reconstituted with Slug−/− HSC is similar to that for Slug−/−mice. A representative analysis of the c-kit+ cells present in the BM and spleen of normal recipient mice reconstituted with either Slug+/+ HSC or Slug−/− HSC after the induction of hemolytic anemia with PHZ is shown.

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