Sample information curated by ChIP-Atlas

Antigen

Antigen Class
No description
Antigen
NA

Cell type

Cell type Class
Neural
Cell type
Hippocampus
MeSH Description
A curved elevation of GRAY MATTER extending the entire length of the floor of the TEMPORAL HORN of the LATERAL VENTRICLE (see also TEMPORAL LOBE). The hippocampus proper, subiculum, and DENTATE GYRUS constitute the hippocampal formation. Sometimes authors include the ENTORHINAL CORTEX in the hippocampal formation.

Attributes by original data submitter

Sample

ENA first public
2020-04-17
ENA last update
2020-04-16
ENA-CHECKLIST
ERC000011
External Id
SAMEA6787271
INSDC center alias
BCM
INSDC center name
Baylor College of Medicine
INSDC first public
2020-04-17T04:05:27Z
INSDC last update
2020-04-16T18:11:22Z
INSDC status
public
Submitter Id
E-MTAB-8954:65.IN.SAL.ACTGAT
age
3 to 4
broker name
ArrayExpress
common name
house mouse
developmental stage
adult
genotype
wild type genotype
individual
65
organism part
hippocampus
sample name
E-MTAB-8954:65.IN.SAL.ACTGAT
sex
male
strain
C57BL/6
weeks after injection
5 week

Sequenced DNA Library

library_name
65.IN.SAL.ACTGAT_s
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
To verify that hippocampal samples used for ΔFosB ChIP-seq came from mice with seizures and high ΔFosB expression, we first performed immunohistochemistry (Cell Signaling, D3S8R) to detect ΔFosB in one hemibrain (right side). We isolated the entire hippocampal formation from each mouse by chilling each hemibrain (left side) on an ice block, and rolling out the entire hippocampal formation using a molt elevator (Roboz, RS-8830). To perform ChIP, after removing 2% of sheared chromatin samples to use as input, chromatin fragments bound to ΔFosB were isolated using a rabbit anti-ΔFosB antibody (Cell Signaling, D3S8R), with normal rabbit IgG (Millipore 12-370) used as a negative control. All antibody concentrations were 2 μg/reaction, and samples were processed using the Magna ChIP A Kit (Millipore) for pulldown. Library preparation of ~300bp-long ChIP-seq sample fragments (NEBNext Kit, New England Biolabs) was performed by the University of Pennsylvania Next-Generation Sequencing Core prior to Illumina sequencing.

Sequencing Platform

instrument_model
Illumina HiSeq 4000

mm10

Number of total reads
16895249
Reads aligned (%)
93.3
Duplicates removed (%)
41.2
Number of peaks
361 (qval < 1E-05)

mm9

Number of total reads
16895249
Reads aligned (%)
92.6
Duplicates removed (%)
41.1
Number of peaks
443 (qval < 1E-05)

Base call quality data from DBCLS SRA