%0 Figure %A Moraghebi, Roksana %A Kirkeby, Agnete %A Chaves, Patricia %A Rรถnn, Roger %A Sitnicka, Ewa %A Parmar, Malin %A Larsson, Marcus %A Herbst, Andreas %A Woods, Niels-Bjarne %D 2017 %T Additional file 6: of Term amniotic fluid: an unexploited reserve of mesenchymal stromal cells for reprogramming and potential cell therapy applications %U https://springernature.figshare.com/articles/figure/Additional_file_6_of_Term_amniotic_fluid_an_unexploited_reserve_of_mesenchymal_stromal_cells_for_reprogramming_and_potential_cell_therapy_applications/5349580 %R 10.6084/m9.figshare.c.3864190_D6.v1 %2 https://springernature.figshare.com/ndownloader/files/9190711 %K Term amniotic fluid %K Caesarean section deliveries %K Mesenchymal stromal cells %K Cell-based therapy %K Cellular reprogramming %K Pluripotency %K Regenerative medicine %K Biobanking %X Showing TAF-iPS cell lines are pluripotent. (a) Q-RT-PCR analyses of OCT4, SOX2, KLF4, C-MYC, NANOG, DNMT3B, TDGF1 (CRIPTO), and ZFP42 (REX1) expression in nine TAF-iPS, CB-iPS and hES cell lines. Samples were normalized against the internal control (GAPDH) and plotted (log10 scale) relative to the expression level in the hES cell line HUES-3, which is arbitrarily set to a value of 1. (b) Histological analyses of teratomas generated by TAF-iPS cell lines reveal the presence of tissues with characteristic structures of all three germ layers. Representative images of haematoxylin and eosin (H&E)-stained teratoma sections, generated from a TAF-iPS cell line following subcutaneous injection of 500,000 iPS cells into NSG mice. (TIF 14420 kb) %I figshare