Sample information curated by ChIP-Atlas

Antigen

Antigen Class
TFs and others
Antigen
POU2F1

Cell type

Cell type Class
Prostate
Cell type
Prostatic Neoplasms, Castration-Resistant
MeSH Description
Tumors or cancer of the PROSTATE which can grow in the presence of low or residual amount of androgen hormones such as TESTOSTERONE.

Attributes by original data submitter

Sample

source_name
AR-positive CRPC cells
cell type
AR-positive CRPC cells
culture
2D cultured from PDX
treatment
DHT 10 nM for 24 h + PI for 48 h
chip antibody
OCT1 (abcam 15112)

Sequenced DNA Library

library_name
GSM5772720
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. The Chromatin immunoprecipitated DNA fragments (approx.10 ng in 30 µl water) are end repaired by using T4 DNA polymerase, Klenow DNA polymerase and T4 polynucleotide kinase in the presence of dNTPs. And an 'A' base is added to the 3'end of the blunt phosphorylated DNA fragments, using the polymerase activity of Klenow fragment. Then, adaptors (Adaptor oligo mix, Illumina) are ligated to the ends of the DNA fragments. The resulting DNA fragments are purified by MinElute column (QIAGEN). 300 ~ 500 bp DNA fragments are purified by using E-Gel SizeSelect agarose Gels (Invitrogen) according to manufacturer's instruction. Size selected adaptor-modified DNA fragments are amplifiedand the resulting PCR products are purified by MinElute column (QIAGEN). The size and amount of DNA fragments (libraries) are validated by Bioanalyzer (Agilent).

Sequencing Platform

instrument_model
Illumina NovaSeq 6000

hg38

Number of total reads
30367426
Reads aligned (%)
4.4
Duplicates removed (%)
32.0
Number of peaks
161 (qval < 1E-05)

hg19

Number of total reads
30367426
Reads aligned (%)
4.4
Duplicates removed (%)
32.4
Number of peaks
166 (qval < 1E-05)

Base call quality data from DBCLS SRA