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Status |
Public on Apr 05, 2016 |
Title |
H3K4me3 ChIP in multiple myeloma MM1S cells in the presence and absence of KDM5-C70 |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
In this experiment we demonstrate the use of an inhibitor of the KDM5 family of histone demethylases, KDM5-C70, on H3K4me3 marks in the multiple myeloma cell line MM1S. KDM5-C70 increases H3K4me3 in a global fashion across the genome.
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Overall design |
Examination of H3K4me3 mark across MM1S cells treated with either KDM5-C70 or vehicle control
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Contributor(s) |
Oppermann U, Hookway E |
Citation(s) |
27214403 |
Submission date |
Feb 23, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Udo Oppermann |
Organization name |
University of Oxford
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Department |
Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences
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Street address |
Botnar Research Centre, Nuffield Orthopaedic Centre, Windmill Road
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City |
Oxford |
State/province |
Oxfordshire |
ZIP/Postal code |
OX3 7LD |
Country |
United Kingdom |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (8)
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Relations |
BioProject |
PRJNA312929 |
SRA |
SRP070701 |