Sample information curated by ChIP-Atlas

Antigen

Antigen Class
TFs and others
Antigen
Tcf3

Cell type

Cell type Class
Liver
Cell type
Liver
MeSH Description
A large lobed glandular organ in the abdomen of vertebrates that is responsible for detoxification, metabolism, synthesis and storage of various substances.

Attributes by original data submitter

Sample

source_name
liver tissue
strain
C57BL/6
antibody
E2A (sc-349; LOT:C1115; SantaCruz)
time of day
ZT 10
Sex
male
diet
chow
genotype
E47+/+

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
ChIP was performed as previously described (Quagliarini et al., 2018) with minor changes for pellet preparation. Mouse livers were harvested, snap-frozen and homogenized in lysis buffer (10mM Hepes-KOH, 10mM KCL, 5mM MgCl2, 0.5mM DTT) using the TissueLyser (Qiagen) with steel beads. Lysates were passed through a cell strainer and cross-linked in 1% formaldehyde for 15 min followed by quenching with 0.2 M glycine solution for 5 min. Library preperation was performed from 2 ng of ChIP DNA using the Kapa Hyper Prep Kit with PCR library amplification (#KK8504, KapaBiosystems) according to the manufactur's protocol. Shortly, ChIP DNA was end-repaired and A-tailed before adapter ligation. After adapter ligation, the ChIP DNA was purified with Agencourt AMPure XP beads (#A63880, Beckman Coulter) and size-selected for 360-600 bp using the Pippin Prep System from Saga Science. The size-selected library is amplified by PCR using the Kapa Hyper Prep Kit (#KK8504,KapaBiosystems) and purified terminally with Agencourt AMPure XP beads (#A63880, Beckman Coulter).

Sequencing Platform

instrument_model
Illumina HiSeq 4000

mm10

Number of total reads
41481309
Reads aligned (%)
98.2
Duplicates removed (%)
35.9
Number of peaks
507 (qval < 1E-05)

mm9

Number of total reads
41481309
Reads aligned (%)
98.1
Duplicates removed (%)
35.8
Number of peaks
458 (qval < 1E-05)

Base call quality data from DBCLS SRA