Abstract
The KCL012 human embryonic stem cell line was derived from an embryo donated for research that carried an autosomal dominant mutation affecting one allele of the HTT gene encoding huntingtin (46 trinucleotide repeats; 17 for the normal allele). The ICM was isolated using laser microsurgery and plated on γ-irradiated human foreskin fibroblasts. Both the derivation and cell line propagation were performed in an animal product-free environment. Pluripotent state and differentiation potential were confirmed by in vitro and in vivo assays.
Original language | English |
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Pages (from-to) | 264-267 |
Number of pages | 4 |
Journal | Stem Cell Research |
Volume | 16 |
Issue number | 2 |
Early online date | 14 Jan 2016 |
DOIs | |
Publication status | Published - Mar 2016 |