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Status |
Public on Sep 24, 2013 |
Title |
Genome wide ChIP-Seq profiles of p300 and CBP in control and cells expressing HSP70K71E |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
There were more enriched p300 and CBP bindings at the promoter regions in the cells expresing HSP70K71E compared to the control
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Overall design |
HEK293 cells were overexpressed with pCI1-EGFP (control) and with HSP70K71E-EGFP (mutant) and appied for ChIP-Seq.
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Contributor(s) |
Byun JS, Gardner K |
Citation missing |
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Submission date |
Sep 24, 2013 |
Last update date |
May 15, 2019 |
Contact name |
Jung S Byun |
E-mail(s) |
byunjs@mail.nih.gov
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Phone |
3014352890
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Organization name |
NCI/NIH
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Lab |
Genetics Branch
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Street address |
37 convent drive, Bldg 37, Rm 1042
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City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892 |
Country |
USA |
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Platforms (1) |
GPL10999 |
Illumina Genome Analyzer IIx (Homo sapiens) |
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Samples (10)
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This SubSeries is part of SuperSeries: |
GSE51118 |
p300 is a preferred client protein for Nuclear Chaperones |
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Relations |
BioProject |
PRJNA221229 |
SRA |
SRP030398 |