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Original

Collagen as an Immobilization Vehicle for Bone Marrow Stromal Cells Enriched with Osteogenic Potential

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Pages 59-68 | Published online: 24 Aug 2009

Figures & data

Figure 1. The cell numbers were counted during the culture periods. Collagen‐coated dishes are reconstituted in incubator at 37°C (•) or let dried under laminar flow (♦).

Figure 1. The cell numbers were counted during the culture periods. Collagen‐coated dishes are reconstituted in incubator at 37°C (•) or let dried under laminar flow (♦).

Figure 2. The alkaline phosphatase activities were measured during the culture periods. Collagen‐coated dishes are reconstituted in incubator at 37°C (•) or let dried under laminar flow (♦).

Figure 2. The alkaline phosphatase activities were measured during the culture periods. Collagen‐coated dishes are reconstituted in incubator at 37°C (•) or let dried under laminar flow (♦).

Figure 3. Alkaline phosphatase staining of stromal cells that grown on collagen‐coated glass plate for 7‐days. The presence of alkaline phosphatase in the cytoplasm is displayed as violet red color.

Figure 3. Alkaline phosphatase staining of stromal cells that grown on collagen‐coated glass plate for 7‐days. The presence of alkaline phosphatase in the cytoplasm is displayed as violet red color.

Figure 4. The von Kossa staining of the cells on conventional dish (A) and collagen‐coated dish (B) after 2 weeks culture.

Figure 4. The von Kossa staining of the cells on conventional dish (A) and collagen‐coated dish (B) after 2 weeks culture.

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