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. 2010 Nov 23;5(11):e14099. doi: 10.1371/journal.pone.0014099

Figure 7. In vitro differentiation using embryoid bodies from hiPSCs generated and maintained in defined culture conditions.

Figure 7

Immunohistochemistry of MAP2 (A), TUJ (B), FLK1 (C), VIMENTIN (D), and PDX1 (E) in the differentiated hiPSC line, UTA-SF-2-2, grown under hESF9a-based conditions. Differentiation was performed using embryoid body formation. The tissues in embryoid bodies were fixed and reacted with antibodies. Binding of these antibodies was visualized with AlexaFluor 488-conjugated secondary antibodies (green). Nuclei were stained with DAPI (blue). Scale bars are 50 µm.