Sample information curated by ChIP-Atlas

Antigen

Antigen Class
TFs and others
Antigen
BRD4

Cell type

Cell type Class
Kidney
Cell type
HEK293-T-REx
Tissue
kidney
Lineage
mesoderm
Description
embryonic kidney cells transformed with Adenovirus 5 DNA stably expressing tetracycline repressor, HEK293 (ATCC number CRL-1573) is the parental cell line, hypotriploid, XXX

Attributes by original data submitter

Sample

source_name
293Trex
chip antibody
BRD4-NUT (anti-NUT, 15 ul per IP; Cell Signaling, catalog no. 3625)
cell type
293Trex (cells originating from embryonic kidney)
cell line
293Trex_B4Nflag
treatment
3h -incubation time period with Tetracycline (final concentration of 1ug/ml).

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Formaldehyde cross-linked chromatin for ChIP-seq experiments with antibodies against proteins and histone modifications were prepared from 1.5 × 108 cells of each NMC cell line and 293TRex-Flag-BRD4NUT-HA as described (Alekseyenko et al. 2015). Chromatin from 0.8g of 1015 patient tissue ((Grayson et al. 2014) was prepared as follows: frozen tissue was ground to a powder with a ceramic mortar and pestle chilled with liquid N2. The powder was immediately transferred into a 50 ml Falcon tube filled with 9mL of NEB buffer (10% sucrose, 20 mM HEPES at pH 7.6, 10 mM NaCl, 3 mM MgCl2, 0.5% Triton, 0.1 mM PMSF). The mixture was vortexed for 15sec to brake-up the clumps, and immediately after, 45 mL of PBS and 0.5mL of 37% formaldehyde were added to the tube. The resulting mixture was incubated for 25 min at 25°C on an orbital shaker platform with gentle mixing (150 rpm). Washing and chromatin shearing steps were performed as described (Alekseyenko et al. 2015). Affinity purification was performed as described (Kharchenko et al. 2011). Input and IP DNA recovery and ChIP-seq library preparation were performed as described (Alekseyenko et al. 2015). The following antibodies against proteins and histone modifications were used for ChIP-seq experiments: anti-H3K27ac (10 ul per IP, Active Motif, catalog no. 39133); anti-H3K9ac (15 ul per IP, Abcam, catalog no. ab12179); anti-H3K14ac (2 ul per IP, Abcam , catalog no. ab52946), anti-H3K36me3 (3 ul per IP, Abcam , catalog no. ab9050) anti-P300 (10 ul, Bethyl, catalog no. A300-358A); anti-BRD4-SL (against short and long isoforms of BRD4, 5 ul per IP, Bethyl, catalog no. A301-985A), anti-BRD4-L (against long isoforms of BRD4, 15 ul per IP, Active Motif, catalog no. 39909); anti-NUT (15 ul per IP; Cell Signaling, catalog no. 3625). ChIP-seq library preparation were performed as described (Alekseyenko et al. 2015).

Sequencing Platform

instrument_model
Illumina HiSeq 2500

hg38

Number of total reads
11190924
Reads aligned (%)
98.4
Duplicates removed (%)
0.7
Number of peaks
251 (qval < 1E-05)

hg19

Number of total reads
11190924
Reads aligned (%)
97.8
Duplicates removed (%)
0.8
Number of peaks
244 (qval < 1E-05)

Base call quality data from DBCLS SRA