<p>hESCs were first maintained in E8 Medium with either bFGF (A) or FGFC (B) and then prepared for the <i>in vitro</i> differentiation assay. Differentiation into three germ lineages (neural, muscle, and liver) was detected by immunocytochemistry. The result of a single experiment is shown. TUJ1: anti-Class IIIβ-Tubulin, SMA: anti-human smooth muscle actin, AFP: anti-α-fetoprotein. no 1° Ab: negative control cells stained with each secondary antibody alone. Scale bar: 100 μm.</p
<p>H5 884 cells treated with Plasmocin<sup>TM</sup> 25 µg/ml during 14 days (Curative treatment) and...
<p>(<b>A</b>) hESC line NCL3 and (<b>B</b>) iPS line 1 were cultured for 3 passages in FTDA, in MEF-...
<p>(<b>A</b>) Directed <i>in vitro</i> differentiation of three GMP-transitioned RiPSC lines into th...
<p>H9 hES cells on Matrigel were cultured for at least six passages in either NM23-H1-MM (minimal st...
<p>(A-D) Pluripotent marker expression in H1 ESCs cultured in E8 Medium with bFGF (A), FGFC (B), or ...
<p>A, Immunostaining showing that markers for the three germ layers (α-smooth muscle actin, α-fetopr...
<p>a, b) H9 ES cells and iPS cells serially passaged on a monoclonal anti-MUC1* antibody surface in ...
<p>(A): EBs were generated from HDF or ASC derived iPSCs by suspension culture, and auto-differentia...
<p>(A) iPSC lines were derived and assessed for pluripotency markers (B) iPSCs grown for two weeks o...
Establishing a model for in vitro differentiation of human embryo-nic stem cells (hESCs) towards the...
<p>WA09 hES cells were cultured for three days on Matrigel coated dishes in the indicated medium (un...
<p>(A) Embryoid body formation of pbiPSCs grown for 6 days in low cell-adhesion dishes. Immunocytoch...
shRNA control, Clone 1 and Clone 2 were let to differentiate until day 10. Differentiation into the ...
<p>The hESCs colonies had the typical morphology of human pluripotent stem cell colonies with clear ...
<p>(A and B) H9 human ES cells were induced to differentiate into the hepatic lineage on R-Fc- or NC...
<p>H5 884 cells treated with Plasmocin<sup>TM</sup> 25 µg/ml during 14 days (Curative treatment) and...
<p>(<b>A</b>) hESC line NCL3 and (<b>B</b>) iPS line 1 were cultured for 3 passages in FTDA, in MEF-...
<p>(<b>A</b>) Directed <i>in vitro</i> differentiation of three GMP-transitioned RiPSC lines into th...
<p>H9 hES cells on Matrigel were cultured for at least six passages in either NM23-H1-MM (minimal st...
<p>(A-D) Pluripotent marker expression in H1 ESCs cultured in E8 Medium with bFGF (A), FGFC (B), or ...
<p>A, Immunostaining showing that markers for the three germ layers (α-smooth muscle actin, α-fetopr...
<p>a, b) H9 ES cells and iPS cells serially passaged on a monoclonal anti-MUC1* antibody surface in ...
<p>(A): EBs were generated from HDF or ASC derived iPSCs by suspension culture, and auto-differentia...
<p>(A) iPSC lines were derived and assessed for pluripotency markers (B) iPSCs grown for two weeks o...
Establishing a model for in vitro differentiation of human embryo-nic stem cells (hESCs) towards the...
<p>WA09 hES cells were cultured for three days on Matrigel coated dishes in the indicated medium (un...
<p>(A) Embryoid body formation of pbiPSCs grown for 6 days in low cell-adhesion dishes. Immunocytoch...
shRNA control, Clone 1 and Clone 2 were let to differentiate until day 10. Differentiation into the ...
<p>The hESCs colonies had the typical morphology of human pluripotent stem cell colonies with clear ...
<p>(A and B) H9 human ES cells were induced to differentiate into the hepatic lineage on R-Fc- or NC...
<p>H5 884 cells treated with Plasmocin<sup>TM</sup> 25 µg/ml during 14 days (Curative treatment) and...
<p>(<b>A</b>) hESC line NCL3 and (<b>B</b>) iPS line 1 were cultured for 3 passages in FTDA, in MEF-...
<p>(<b>A</b>) Directed <i>in vitro</i> differentiation of three GMP-transitioned RiPSC lines into th...