Literature DB >> 27346013

Derivation of Huntington Disease affected Genea091 human embryonic stem cell line.

Biljana Dumevska1, Julia Schaft2, Robert McKernan2, Jesselyn Hu2, Uli Schmidt2.   

Abstract

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.

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Year:  2016        PMID: 27346013     DOI: 10.1016/j.scr.2016.02.022

Source DB:  PubMed          Journal:  Stem Cell Res        ISSN: 1873-5061            Impact factor:   2.020


  1 in total

Review 1.  Cell Reprogramming to Model Huntington's Disease: A Comprehensive Review.

Authors:  Ruth Monk; Bronwen Connor
Journal:  Cells       Date:  2021-06-22       Impact factor: 6.600

  1 in total

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