A: CCK8 assay. The y-axis shows the amount of absorbance, the y-axis the measuring time points. B: The Transwell migration assay results. The y-axis shows the cells number per mm2 and the x-axis shows the different groups. * PC: ASCs and HASCs were underwent 21 days of adipogenic differentiation. The cells were fixed and stained with Oil-Red-O. The images were took by a microscope. Scale bar = 50μm. D: Quantitative analysis of Oil Red O staining. Dye stained cells was extracted with isopropanol and the absorbance at 540 nm was measured. * P<0.05, ***P<0.001, n = 3.</p
<p>(A) Cell culture morphology of differentiated MSCs from control animals cultured in adipogenic me...
<p>(a) ASCs isolated from human subcutaneous adipose tissue adhered to the dish and were spindle- or...
<p>(<b>A</b>): Flow cytometric analysis after the 3<sup>rd</sup> passage of porcine ASCs labelled wi...
<p>(A) ASC were adherent to culture flaks and exhibited a fibroblast-like spindle-shaped morphology....
<p>The morphology of HUCs and ASCs at passage number 3 and ASCs after induction by conditioned mediu...
<p>A. ASCs were cultured in the bottom well of a Boyden Chamber and MDA-MB-231 cells were cultured i...
<p>Phase contrast images of hASCs subjected to a chemically-defined method for differentiation to ad...
<p>A) Transmissive scanning of Oil-Red-O stained high and low adipogenic cells. B) Quantification of...
<p>ASCs cultivated on biomaterials PEUU (A), PEU (B) and PLLA (C) and differentiated for 21 days int...
<p>The ASC were cultured under lipid accumulation stimulus for up to 3 weeks. Lipid accumulation was...
<p>(A) Microscope images of undifferentiated ASCs at passage 3; Alizarin Red-stained osteogenic ASCs...
<p>(A) Before and (B) after Oil red O staining. Treatment conditions were (i) non-induced control me...
<p>(A) Cells were photographed at days 0, 7 and 21 of their adipocytic differentiation after Oil Red...
<p>(a) The morphology of ADSCs after plating for 24 h. Bar = 200 µm. (b) ADSCs achieved a confluenc...
<p>(A) The lipid droplet of cells cultured in adipogenic medium for 21 days. (B) Staining was not ob...
<p>(A) Cell culture morphology of differentiated MSCs from control animals cultured in adipogenic me...
<p>(a) ASCs isolated from human subcutaneous adipose tissue adhered to the dish and were spindle- or...
<p>(<b>A</b>): Flow cytometric analysis after the 3<sup>rd</sup> passage of porcine ASCs labelled wi...
<p>(A) ASC were adherent to culture flaks and exhibited a fibroblast-like spindle-shaped morphology....
<p>The morphology of HUCs and ASCs at passage number 3 and ASCs after induction by conditioned mediu...
<p>A. ASCs were cultured in the bottom well of a Boyden Chamber and MDA-MB-231 cells were cultured i...
<p>Phase contrast images of hASCs subjected to a chemically-defined method for differentiation to ad...
<p>A) Transmissive scanning of Oil-Red-O stained high and low adipogenic cells. B) Quantification of...
<p>ASCs cultivated on biomaterials PEUU (A), PEU (B) and PLLA (C) and differentiated for 21 days int...
<p>The ASC were cultured under lipid accumulation stimulus for up to 3 weeks. Lipid accumulation was...
<p>(A) Microscope images of undifferentiated ASCs at passage 3; Alizarin Red-stained osteogenic ASCs...
<p>(A) Before and (B) after Oil red O staining. Treatment conditions were (i) non-induced control me...
<p>(A) Cells were photographed at days 0, 7 and 21 of their adipocytic differentiation after Oil Red...
<p>(a) The morphology of ADSCs after plating for 24 h. Bar = 200 µm. (b) ADSCs achieved a confluenc...
<p>(A) The lipid droplet of cells cultured in adipogenic medium for 21 days. (B) Staining was not ob...
<p>(A) Cell culture morphology of differentiated MSCs from control animals cultured in adipogenic me...
<p>(a) ASCs isolated from human subcutaneous adipose tissue adhered to the dish and were spindle- or...
<p>(<b>A</b>): Flow cytometric analysis after the 3<sup>rd</sup> passage of porcine ASCs labelled wi...