16 research outputs found

    Adipogenic differentiation.

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    <p>ASCs cultivated on biomaterials PEUU (A), PEU (B) and PLLA (C) and differentiated for 21 days into an adipogenic lineage. Cells are stained with AdipoRed to show fat droplets. Bars represent 100 µm.</p

    ASCs) were differentiated for seven and fourteen days on polymer-coated plates as well as on typical cell culture plates (TCP).

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    <p>Afterwards, expression of 17 genes associated with adipogenesis and lipogenesis was determined by qRT-PCR. All Ct values were normalized to GAPDH. Mean values of expression levels from 2 different donors are depicted relative to undifferentiated cells set as 1.</p

    Cell viability and morphology.

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    <p>ASCs were grown on biomaterial PEUU (A-D), PEU (E-H) and PLLA (I-L) for 48 hours. Viability was detected by fluorescein diacetate (living cells; A, E, I) and ethidium-homodimer-1 (nuclei of dead cells; B, F, J) staining. C, G and K are merged pictures. Morphology was detected by TRITC-phalloidin (cytoskeleton, red) and DAPI (nuclei, blue) staining (D, H, L). Bars represent 100 µm (A-C, E-G, I-K) or 50 µm (D, H, L).</p

    Adipogenic differentiation.

    No full text
    <p>ASCs cultivated on biomaterials PEUU (A), PEU (B) and PLLA (C) and differentiated for 21 days into an adipogenic lineage. Cells are stained with AdipoRed to show fat droplets. Bars represent 100 µm.</p
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