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SRX2606566: GSM2516782: CHL1_BRD4q_DMSO_01; Homo sapiens; ChIP-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 93.4M spots, 23G bases, 8.6Gb downloads

Submitted by: NCBI (GEO)
Study: ChIPSeq data from melanoma cancer cell line CHL-1 after Bromodomain and extra terminal (Bet) domain inhibitor treatment
show Abstracthide Abstract
Bromodomain and extra terminal domain (BET) inhibition reduces occupancy of BET-family proteins at promoter and enhancer sites finally leading to genome wide changes in gene transcription. We used ChIPSeq profiling to investigate genome wide changes in promoter and enhancer occupancy induced by BET inhibitors BAY 1238097 and OTX-015, respectively. Overall design: CHL-1 cells were treated with BAY 1238097 or OTX-015, potent and selective Bromodomain and extra terminal domain (BET) inhibitors, before chromatin immunoprecipitation using antibodies directed against BRD4 and acetylated H3K27.
Sample: CHL1_BRD4q_DMSO_01
SAMN06470137 • SRS2017431 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: Illumina HiSeq 2500
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: PAIRED
Construction protocol: One 15 cm cell culture dish with 80% confluent cells was used per IP. ChIP DNA preparation for sequencing was carried out as described previously in Nagarajan et al. (Cell Rep. 2014 Jul 24;8(2):460-9) with the following changes: cross-linked chromatin was sheared to 200-800 base pair fragments using sonication (30 sec on/30 sec off, high power, 2 x 7.5 minutes with a water bath change between the two cycles) in a Biorupter sonicator UCD-200. 1.5 µg antibodies (anti-BRD4 [Bethyl Labs, A301-985A100]; anti-H3K27ac [Diagenode, C15410174]) were used per IP. DNA was purified using a PCR purification kit (Qiagen) TrueSeq® ChIP Sample Preparation Guide (Illumina).
Experiment attributes:
GEO Accession: GSM2516782
Links:
Runs: 1 run, 93.4M spots, 23G bases, 8.6Gb
Run# of Spots# of BasesSizePublished
SRR530512893,407,49723G8.6Gb2017-10-11

ID:
3769372

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