Figure 2
Figure 2. Scl haplodeficiency decreases mean stem cell activity. (A) Experimental scheme. Bone marrow cells from adult Scl+/− mice and Scl+/+ littermates or age-matched controls were processed in parallel. (B) Western blot of total protein extracts were used to assess SCL and E2A protein levels in Scl+/+ and Scl+/− lineage-depleted bone marrow cells. Anti-PTP1D was used as a loading control. Ratio of chemiluminescent intensities from Scl+/− over Scl+/+ samples are shown on the right. (C) The frequency of LT-HSCs in Scl+/+ and Scl+/− mice was assessed by flow cytometric analysis of Kit+Sca1+Lin−CD150+CD48− cells. Shown are box plots with the median and extreme values of each distribution (n mice per group). The 2 distributions are not significantly different (P = .1). (D) The mean stem cell activity (MAS) was calculated in mice receiving approximately 1 CRU, as described in “Transplantation assays.” Box plots as above from n mice; P values as shown.

Scl haplodeficiency decreases mean stem cell activity. (A) Experimental scheme. Bone marrow cells from adult Scl+/− mice and Scl+/+ littermates or age-matched controls were processed in parallel. (B) Western blot of total protein extracts were used to assess SCL and E2A protein levels in Scl+/+ and Scl+/− lineage-depleted bone marrow cells. Anti-PTP1D was used as a loading control. Ratio of chemiluminescent intensities from Scl+/− over Scl+/+ samples are shown on the right. (C) The frequency of LT-HSCs in Scl+/+ and Scl+/− mice was assessed by flow cytometric analysis of Kit+Sca1+LinCD150+CD48 cells. Shown are box plots with the median and extreme values of each distribution (n mice per group). The 2 distributions are not significantly different (P = .1). (D) The mean stem cell activity (MAS) was calculated in mice receiving approximately 1 CRU, as described in “Transplantation assays.” Box plots as above from n mice; P values as shown.

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