Derivation of Huntington Disease affected Genea018 human embryonic stem cell line
The Genea018 human embryonic stem cell line was derived from a donated, fully commercially consented ART blastocyst, carrying Htt gene CAG expansion of 46 repeats, indicative of Huntington Disease. Following ICM outgrowth on inactivated human feeders, karyotype was confirmed as 46, XX by CGH and STR...
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2016-03-01
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Series: | Stem Cell Research |
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doaj-48ffee8d16fa41ce9ccd808f1954a62e2020-11-24T23:06:35ZengElsevierStem Cell Research1873-50611876-77532016-03-0116242342610.1016/j.scr.2016.02.006Derivation of Huntington Disease affected Genea018 human embryonic stem cell lineBiljana DumevskaHeather MainRobert McKernanDivya GoelUli SchmidtTeija PeuraThe Genea018 human embryonic stem cell line was derived from a donated, fully commercially consented ART blastocyst, carrying Htt gene CAG expansion of 46 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, 75% of cells expressed Nanog, 91% Oct4, 73% Tra1-60 and 96% SSEA4, gave a Pluritest pluripotency score of 31.12, Novelty of 1.45, demonstrated Alkaline Phosphatase activity and tri-lineage teratoma formation. The cell line was negative for Mycoplasma and visible contamination.http://www.sciencedirect.com/science/article/pii/S1873506116000489 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Biljana Dumevska Heather Main Robert McKernan Divya Goel Uli Schmidt Teija Peura |
spellingShingle |
Biljana Dumevska Heather Main Robert McKernan Divya Goel Uli Schmidt Teija Peura Derivation of Huntington Disease affected Genea018 human embryonic stem cell line Stem Cell Research |
author_facet |
Biljana Dumevska Heather Main Robert McKernan Divya Goel Uli Schmidt Teija Peura |
author_sort |
Biljana Dumevska |
title |
Derivation of Huntington Disease affected Genea018 human embryonic stem cell line |
title_short |
Derivation of Huntington Disease affected Genea018 human embryonic stem cell line |
title_full |
Derivation of Huntington Disease affected Genea018 human embryonic stem cell line |
title_fullStr |
Derivation of Huntington Disease affected Genea018 human embryonic stem cell line |
title_full_unstemmed |
Derivation of Huntington Disease affected Genea018 human embryonic stem cell line |
title_sort |
derivation of huntington disease affected genea018 human embryonic stem cell line |
publisher |
Elsevier |
series |
Stem Cell Research |
issn |
1873-5061 1876-7753 |
publishDate |
2016-03-01 |
description |
The Genea018 human embryonic stem cell line was derived from a donated, fully commercially consented ART blastocyst, carrying Htt gene CAG expansion of 46 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, 75% of cells expressed Nanog, 91% Oct4, 73% Tra1-60 and 96% SSEA4, gave a Pluritest pluripotency score of 31.12, Novelty of 1.45, demonstrated Alkaline Phosphatase activity and tri-lineage teratoma formation. The cell line was negative for Mycoplasma and visible contamination. |
url |
http://www.sciencedirect.com/science/article/pii/S1873506116000489 |
work_keys_str_mv |
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1725622395120648192 |