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Status |
Public on Sep 20, 2015 |
Title |
Catalytically inactive Ring1B maintains near wildtype levels of gene expression in mESCs |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
This experiment was designed to determine the extent of gene misregulation in mESCs containing catalytically dead Ring1B in comparison to mESCs lacking Ring1B.
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Overall design |
Polyadenylated mRNA was prepared from wildtype mESCs (WT), mESCs deficient for Ring1B (KO) and mESCs cells containing catalytically dead Ring1B (I53A). Each sample is represented by 3 biological replicate hybridisations.
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Contributor(s) |
Moffat M, Illingworth RS, Wilson A, Read D, Marulasiddappa PM, Adams I, Bickmore WA |
Citation(s) |
26385961 |
Submission date |
Jun 12, 2015 |
Last update date |
Feb 02, 2018 |
Contact name |
Rob S Illingworth |
E-mail(s) |
robert.illingworth@ed.ac.uk
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Phone |
01316519640
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Organization name |
The University of Edinburgh
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Department |
Centre for regenerative Medicine
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Lab |
Illingworth
|
Street address |
Centre for Regenerative Medicine
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City |
Edinburgh |
State/province |
Midlothian |
ZIP/Postal code |
EH16 4UU |
Country |
United Kingdom |
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Platforms (1) |
GPL10787 |
Agilent-028005 SurePrint G3 Mouse GE 8x60K Microarray (Probe Name version) |
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Samples (9)
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This SubSeries is part of SuperSeries: |
GSE69978 |
Loss of Ring1B catalytic activity causes a pronounced reduction in H3K27me3 deposition yet minimally disrupts the expression of target genes |
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Relations |
BioProject |
PRJNA286873 |