Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditions
KISCOi001-A is a healthy feeder-free and fully characterized human induced pluripotent stem (iPS) cell line cultured under xeno-free and defined conditions. The cell line is generated from normal human foreskin fibroblasts with non-integrating episomal plasmid vectors encoding OCT4, SOX2, KLF4, NANO...
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doaj-5fafaa6bf96d49ac9d2a8ba7b16738412021-03-13T04:22:19ZengElsevierStem Cell Research1873-50612021-03-0151102193Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditionsJose Inzunza0Jonathan Arias-Fuenzalida1Juan Segura-Aguilar2Ivan Nalvarte3Mukesh Varshney4Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, SwedenDepartment of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden; Centre for Cancer Cell Reprogramming, Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, NorwayMolecular and Clinical Pharmacology ICBM Faculty of Medicine, University of Chile, ChileDepartment of Biosciences and Nutrition, Karolinska Institutet, Huddinge, SwedenDepartment of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden; Corresponding author.KISCOi001-A is a healthy feeder-free and fully characterized human induced pluripotent stem (iPS) cell line cultured under xeno-free and defined conditions. The cell line is generated from normal human foreskin fibroblasts with non-integrating episomal plasmid vectors encoding OCT4, SOX2, KLF4, NANOG, LIN28, nontransforming L-MYC and dominant negative p53. The generated iPS cells are transgene-free and their pluripotency is confirmed by the expression of stem cell markers and capacity to differentiate into the cells of ectoderm, endoderm and mesoderm while their identity and karyotype stability is confirmed with Genomic assays.http://www.sciencedirect.com/science/article/pii/S1873506121000398 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jose Inzunza Jonathan Arias-Fuenzalida Juan Segura-Aguilar Ivan Nalvarte Mukesh Varshney |
spellingShingle |
Jose Inzunza Jonathan Arias-Fuenzalida Juan Segura-Aguilar Ivan Nalvarte Mukesh Varshney Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditions Stem Cell Research |
author_facet |
Jose Inzunza Jonathan Arias-Fuenzalida Juan Segura-Aguilar Ivan Nalvarte Mukesh Varshney |
author_sort |
Jose Inzunza |
title |
Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditions |
title_short |
Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditions |
title_full |
Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditions |
title_fullStr |
Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditions |
title_full_unstemmed |
Generation of nonviral integration-free human iPS cell line KISCOi001-A from normal human fibroblasts, under defined xeno-free and feeder-free conditions |
title_sort |
generation of nonviral integration-free human ips cell line kiscoi001-a from normal human fibroblasts, under defined xeno-free and feeder-free conditions |
publisher |
Elsevier |
series |
Stem Cell Research |
issn |
1873-5061 |
publishDate |
2021-03-01 |
description |
KISCOi001-A is a healthy feeder-free and fully characterized human induced pluripotent stem (iPS) cell line cultured under xeno-free and defined conditions. The cell line is generated from normal human foreskin fibroblasts with non-integrating episomal plasmid vectors encoding OCT4, SOX2, KLF4, NANOG, LIN28, nontransforming L-MYC and dominant negative p53. The generated iPS cells are transgene-free and their pluripotency is confirmed by the expression of stem cell markers and capacity to differentiate into the cells of ectoderm, endoderm and mesoderm while their identity and karyotype stability is confirmed with Genomic assays. |
url |
http://www.sciencedirect.com/science/article/pii/S1873506121000398 |
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