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. Author manuscript; available in PMC: 2023 Feb 7.
Published in final edited form as: Stem Cell Res. 2022 Dec 31;66:103013. doi: 10.1016/j.scr.2022.103013
Unique stem cell line identifier NCHi009-A
Alternative name(s) of stem cell line NCH78
Institution Center for Cardiovascular Research, Abigail Wexner Research Institute, Nationwide Children’s Hospital, Columbus, OH
Contact information of distributor Mingtao Zhao, PhD
Type of cell line iPSC
Origin Human
Additional origin info required for human ESC or iPSC Age: 20 years
Sex: Female
Ethnicity if known: Caucasian
Cell Source Peripheral Blood Mononuclear Cells (PBMCs)
Clonality Clonal
Method of reprogramming Sendai virus vector expressing human KLF4, OCT3/4, SOX2, and c-MYC
Genetic Modification Yes
Type of Genetic Modification Spontaneous mutation
Evidence of the reprogramming transgene loss (including genomic copy if applicable) RT-PCR for Kos transgene (Supplementary Fig. 1B)
Associated disease Hypoplastic left heart syndrome (HLHS)
Gene/locus NOTCH1: c.2058G > A (p.Gly661Ser) / chr9:136515323
Date archived/stock date 31st October 2022
Cell line repository/bank NCHi009-A (NCH78) is deposited in the iPSC repository of pediatric cardiovascular disease in the Center for Cardiovascular Research at the Abigail Wexner Research Institute at Nationwide Children’s Hospital in Columbus, OH, USA. https://hpscreg.eu/cell-line/NCHi009-A
Ethical approval Generation of this iPSC line was under an approved Institutional Review Board (IRB) protocol STUDY00001788 “iPSC Repository of Pediatric Cardiovascular Disease” at Nationwide Children’s Hospital.