Figure 5.
Figure 5. Colony-forming potential of Scl-/- FLK-1+ EB-derived cells. (A) Blast colony (□) and core colony (▦) development from FLK-1+ day 3 Scl+/+ and day 3.5 Scl-/- EBs. Data are presented as mean number of blast colonies and cores per 105 input cells from 3 dishes. (B) Photographs of Scl+/+ blast colonies and Scl-/- cores at day 2 and 3 of development. Original magnification, × 200. Objective × 20, numerical aperture 0.30. MagnaFire software was used to analyze the images. (C) RT-PCR analysis of Scl+/+ (+/+) and Scl-/- (-/-) colonies at days 2 and 3 of growth. Each lane represents a pool of 500 colonies. Hybridization was carried out with probes designed against the 3′ UTR of the indicated genes. (D) Immunohistochemistry of adhesive cells generated from Scl+/+ blast colonies (Scl+/+) and Scl-/- cores (Scl-/-). CD31+ (red) and SMA+ (green) populations are indicated. Original magnification, × 200. Objective × 20, numerical aperture 0.70. OpenLab software was used to analyze the images.

Colony-forming potential of Scl-/- FLK-1+ EB-derived cells. (A) Blast colony (□) and core colony (▦) development from FLK-1+ day 3 Scl+/+ and day 3.5 Scl-/- EBs. Data are presented as mean number of blast colonies and cores per 105 input cells from 3 dishes. (B) Photographs of Scl+/+ blast colonies and Scl-/- cores at day 2 and 3 of development. Original magnification, × 200. Objective × 20, numerical aperture 0.30. MagnaFire software was used to analyze the images. (C) RT-PCR analysis of Scl+/+ (+/+) and Scl-/- (-/-) colonies at days 2 and 3 of growth. Each lane represents a pool of 500 colonies. Hybridization was carried out with probes designed against the 3′ UTR of the indicated genes. (D) Immunohistochemistry of adhesive cells generated from Scl+/+ blast colonies (Scl+/+) and Scl-/- cores (Scl-/-). CD31+ (red) and SMA+ (green) populations are indicated. Original magnification, × 200. Objective × 20, numerical aperture 0.70. OpenLab software was used to analyze the images.

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