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Stem Cell Res ; 31: 174-180, 2018 08.
Artigo em Inglês | MEDLINE | ID: mdl-30099333

RESUMO

Four human iPSC cell lines (one Jervell and Lange-Nielsen Syndrome, one Long QT Syndrome-type 1 and two healthy controls) were generated from peripheral blood obtained from donors belonging to the same family. CytoTune™-iPS 2.0 Sendai Reprogramming Kit (containing OCT3/4, KLF4, SOX2 and cMYC as reprogramming factors) was used to generate all cell lines. The four iPSCs have normal karyotype, express pluripotency markers as determined by RT-PCR and flow cytometry and differentiated spontaneously in vitro into cells of the three germ layers, confirming their pluripotent capacity.


Assuntos
Células-Tronco Pluripotentes Induzidas/metabolismo , Síndrome de Jervell-Lange Nielsen/genética , Síndrome do QT Longo/complicações , Diferenciação Celular , Humanos , Síndrome de Jervell-Lange Nielsen/patologia , Fator 4 Semelhante a Kruppel
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