Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Embryonic fibroblast
Cell type
NIH/3T3
Primary Tissue
Embryo
Tissue Diagnosis
Normal

Attributes by original data submitter

Sample

source_name
NIH3T3 cells
cell line
NIH3T3
treatment
none
antibody
none
replicate
input

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
For FAIRE: Nuclei of formaldehyde crosslinked cells were isolated, lysed and sonicated. Accessible DNA was isolated from the clarified lysates by phenol-chloroform extraction. For ChIP-seq: Nuclei of formaldehyde crosslinked cells were isolated, lysed and sonicated. H3K27ac-DNA complexes were isolated from the clarified lysates with antibody against H3K27ac. For RNA-seq: RNA from harvested cells were column purified with Purelink RNA Mini kit (12183025, life technologies). Libraries were prepared according to Illumina's instructions.

Sequencing Platform

instrument_model
Illumina HiSeq 2000

mm10

Number of total reads
74799549
Reads aligned (%)
97.0
Duplicates removed (%)
13.8
Number of peaks
584 (qval < 1E-05)

mm9

Number of total reads
74799549
Reads aligned (%)
96.8
Duplicates removed (%)
13.8
Number of peaks
699 (qval < 1E-05)

Base call quality data from DBCLS SRA