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. Author manuscript; available in PMC: 2013 Sep 10.
Published in final edited form as: J Genet Genomics. 2010 Apr;37(4):241–248. doi: 10.1016/S1673-8527(09)60042-4

Fig. 4.

Fig. 4

iPS in vitro differentiated to adipocytes. A: EBs formed from human iPS colonies which were expanded over SNL feeders for 15 passages and grown in suspension culture in ultra-low-attachment dishes without bFGF for about 2 weeks. Right and left panels represent EBs under higher magnification (100 ×) and lower magnification (50 ×), respectively. Scale bar = 50 μm (left) or 20 μm (right). B: Oil Red O staining of adipocytes derived from human iPS cells when induced by adipose culture medium for 3 weeks. Nuclei are stained black/blue with the hematoxylin. Right and left panels represent adipocytes by Oil Red O staining under higher magnification (400 ×) and lower magnification (200 ×), respectively. Scale bar = 20 μm (left) or 10 μm (right).