Sample information curated by ChIP-Atlas

Antigen

Antigen Class
TFs and others
Antigen
MAML3

Cell type

Cell type Class
Neural
Cell type
SK-N-SH
Primary Tissue
Brain
Tissue Diagnosis
Neuroblastoma

Attributes by original data submitter

Sample

source_name
Neuroblastoma SK-N-SH control cells, RA treated
cell type
human neuroblastoma cells
cell line
SK-N-SH
chip antibody
MAML3, Bethyl Laboratories, Cat No. A300-684A
treatment
RA treated

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. Libraries were prepared according to Illumina's instructions accompanying the DNA Sample Kit (Part# 0801-0303). Briefly, DNA was end-repaired using a combination of T4 DNA polymerase, E. coli DNA Pol I large fragment (Klenow polymerase) and T4 polynucleotide kinase. The blunt, phosphorylated ends were treated with Klenow fragment (32 to 52 exo minus) and dATP to yield a protruding 3- 'A' base for ligation of Illumina's adapters which have a single 'T' base overhang at the 3’ end. After adapter ligation DNA was PCR amplified with Illumina primers for 15 cycles and library fragments of ~250 bp (insert plus adaptor and PCR primer sequences) were band isolated from an agarose gel. The purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the Genome Analyzer following the manufacturer's protocols.

Sequencing Platform

instrument_model
Illumina HiSeq 2000

hg38

Number of total reads
12976845
Reads aligned (%)
73.0
Duplicates removed (%)
15.9
Number of peaks
3724 (qval < 1E-05)

hg19

Number of total reads
12976845
Reads aligned (%)
72.4
Duplicates removed (%)
16.7
Number of peaks
3791 (qval < 1E-05)

Base call quality data from DBCLS SRA