<p>(A) Embryoid body formation of pbiPSCs grown for 6 days in low cell-adhesion dishes. Immunocytochemical staining for markers for the three germ-layer in differentiated cells derived from pbiPSCs. α-fetoprotein (B, endoderm), actin smooth muscle (C, mesoderm), and glial fibrillary acidic protein (D, ectoderm) were used as markers. (E) Embryoid body formation by pnbiPSCs. Immunocytochemical staining for α-fetoprotein (F), actin smooth muscle (G), glial fibrillary acidic protein (H). (A), (E), scale bars = 500 μm. (B)–(D), (F)–(H), scale bars = 100 μm.</p
<p>MSCs were differentiated into (A) adipogenic (Oil Red O staining), (B) osteogenic (Von Kossa stai...
<p>(a) Light microscopic images of EB cultured for 10 days. (b) Expressions of the genes representin...
<p>H9 hES cells on Matrigel were cultured for at least six passages in either NM23-H1-MM (minimal st...
<p>(<b>A</b>) Representative embryoid bodies derived from EpiSC-like pES cell lines and piPS cell li...
<p>(A): EBs were generated from HDF or ASC derived iPSCs by suspension culture, and auto-differentia...
<p>The ability of HiPSCs to form EB was demonstrated by dispersing colonies to single cell suspensio...
<p>A) Differentiation was performed using embryoid body formation, and the differentiated iPSCs (DP-...
<p>Immunofluorescent staining of Tuj1 (ectoderm marker), α-smooth muscle actin (α-SMA, mesoderm mark...
<p>(<b>A</b>) Immunofluorescence microscopy images of iNdiPSC-1 and -2-differentiated embryoid bodie...
<p>ESCs were maintained in control conditions (with LIF), in the absence of LIF (differentiation con...
<p><b>A–C</b>) Chondrogenic differentiation. <b>A</b>) Pellet culture: collagen fibers intensively s...
<p>(A) Effects of treatment (EB medium; Non-treated, EB medium+BMP4, EB medium+RA or EB medium +BMP4...
<p>a, b) H9 ES cells and iPS cells serially passaged on a monoclonal anti-MUC1* antibody surface in ...
<p>A, Immunostaining showing that markers for the three germ layers (α-smooth muscle actin, α-fetopr...
MSCs were differentiated into (A) adipogenic (Oil Red O staining), (B) osteogenic (Von Kossa stainin...
<p>MSCs were differentiated into (A) adipogenic (Oil Red O staining), (B) osteogenic (Von Kossa stai...
<p>(a) Light microscopic images of EB cultured for 10 days. (b) Expressions of the genes representin...
<p>H9 hES cells on Matrigel were cultured for at least six passages in either NM23-H1-MM (minimal st...
<p>(<b>A</b>) Representative embryoid bodies derived from EpiSC-like pES cell lines and piPS cell li...
<p>(A): EBs were generated from HDF or ASC derived iPSCs by suspension culture, and auto-differentia...
<p>The ability of HiPSCs to form EB was demonstrated by dispersing colonies to single cell suspensio...
<p>A) Differentiation was performed using embryoid body formation, and the differentiated iPSCs (DP-...
<p>Immunofluorescent staining of Tuj1 (ectoderm marker), α-smooth muscle actin (α-SMA, mesoderm mark...
<p>(<b>A</b>) Immunofluorescence microscopy images of iNdiPSC-1 and -2-differentiated embryoid bodie...
<p>ESCs were maintained in control conditions (with LIF), in the absence of LIF (differentiation con...
<p><b>A–C</b>) Chondrogenic differentiation. <b>A</b>) Pellet culture: collagen fibers intensively s...
<p>(A) Effects of treatment (EB medium; Non-treated, EB medium+BMP4, EB medium+RA or EB medium +BMP4...
<p>a, b) H9 ES cells and iPS cells serially passaged on a monoclonal anti-MUC1* antibody surface in ...
<p>A, Immunostaining showing that markers for the three germ layers (α-smooth muscle actin, α-fetopr...
MSCs were differentiated into (A) adipogenic (Oil Red O staining), (B) osteogenic (Von Kossa stainin...
<p>MSCs were differentiated into (A) adipogenic (Oil Red O staining), (B) osteogenic (Von Kossa stai...
<p>(a) Light microscopic images of EB cultured for 10 days. (b) Expressions of the genes representin...
<p>H9 hES cells on Matrigel were cultured for at least six passages in either NM23-H1-MM (minimal st...