Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Histone
Antigen
H3K27me3

Cell type

Cell type Class
Prostate
Cell type
DU 145
Primary Tissue
Prostate
Tissue Diagnosis
Carcinoma

Attributes by original data submitter

Sample

source_name
DU145 prostate cancer cells
cell line
DU145 prostate cancer cells
genotype/variation
control
chip antibody
Anti-H3K27me3 [rabbit, Cell Signaling, cat# 9733, lot# 5]

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibody. ChIP was performed using HighCell ChIP kit following manufacturers protocol (Diagenode) ChIP-Seq libraries were prepared using standard Illumina protocol. ChIP-enriched DNA samples (10-20 ng) were converted to blunt-ended fragments using a combination of T4 DNA polymerase, E.coli DNA polymerase I large fragment (Klenow polymerase) and T4 polynuleotide kinase (New England BioLabs, NEB). A single A-base was added to fragment ends by Klenow fragment (3' to 5' exo minus; NEB) followed by ligation of Illumina adaptors (Quick ligase, NEB). The adaptor-modified DNA fragments were enriched by PCR using the Illumina PE1.0/PE2.0 primers and Phusion DNA polymerase (NEB). PCR products were size selected using 3% NuSieve agarose gels (Lonza) followed by gel extraction using QIAEX II reagents (QIAGEN). Libraries were quantified using the Bioanalyzer 2100 (Agilent) and each sample was sequenced in a single lane on the Illumina HiSeq 2000 (40 nucleotide read length).

Sequencing Platform

instrument_model
Illumina Genome Analyzer II

hg38

Number of total reads
32876686
Reads aligned (%)
93.3
Duplicates removed (%)
47.6
Number of peaks
6016 (qval < 1E-05)

hg19

Number of total reads
32876686
Reads aligned (%)
92.8
Duplicates removed (%)
48.2
Number of peaks
5619 (qval < 1E-05)

Base call quality data from DBCLS SRA