Derivation of Huntington Disease affected Genea091 human embryonic stem cell line
Summary
The Genea091 human embryonic stem cell line was derived from a donated, fully commercially consented ART blastocyst, carrying Htt gene CAG expansion of 40 repeats, indicative of Huntington Disease. Following ICM outgrowth on inactivated human feeders, karyotype was confirmed as 46, XX by CGH and STR analysis demonstrated a female Allele pattern. The hESC line had pluripotent cell morphology, 92% of cells expressed Nanog, 97% Oct4, 79% Tra1-60 and 98% SSEA4 and gave a Pluritest pluripotency score of 38.36, Novelty of 1.35. The cell line was negative for Mycoplasma and visible contamination. Copyright © 2016 University of Texas at Austin Dell Medical School. Published by Elsevier B.V. All rights reserved.
| Authors | Dumevska B, Schaft J, McKernan R, Hu J, Schmidt U |
|---|---|
| Journal | Stem cell research |
| Publication Date | 2016 Mar;16(2):449-51 |
| PubMed | 27346013 |
| DOI | 10.1016/j.scr.2016.02.022 |