Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Blood
Cell type
Hematopoietic Stem Cells
MeSH Description
Progenitor cells from which all blood cells derived. They are found primarily in the bone marrow and also in small numbers in the peripheral blood.

Attributes by original data submitter

Sample

source_name
hematopoietic stem/progenitor cells from bone marrow
strainn
129P2xC57BL/6J
tissue
bone marrow
genotype
wild type
ChIP
input

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
RNA: Total RNA is extracted using the Qiagen Rneasy micro kit. ChIP: ChIP on native chromatin from hematopoitic stem/progenitor cells was performed following previously published protocols (M. Girardot et al., 2014. Nucleic acids research 42, 235-248) with the following modifications using ChIP-grade Magna protein A/G beads (Cat#: 16-663, EMB Millipore). The isolated nuclei were incubated for 15 min at 37°C with 4 units/uL of Micrococcal nuclease (M0247, New England Biolabs) to produce mono/di-nucleosomes as verified by agarose gel electrophoresis. Nucleosomes were precipitated with control IgG, ChIP-grade anti-H4R3me2s (Cat#: Ab5823, Abcam) or anti-H3K9me2s (Cat#: 39375, Active motif). ChIP or input DNA was purified with Ampure XP beads (Cat#: A63880, Beckman Coulter). ChIP libraries were repard according to standard Illumina protocols. Transcriptome libraries were constructed with TruSeq RNA Sample Preparation Kit V2 (Illumia) with minor modifications.

Sequencing Platform

instrument_model
Illumina HiSeq 2500

mm10

Number of total reads
73026330
Reads aligned (%)
98.4
Duplicates removed (%)
12.5
Number of peaks
304 (qval < 1E-05)

mm9

Number of total reads
73026330
Reads aligned (%)
98.2
Duplicates removed (%)
12.5
Number of peaks
315 (qval < 1E-05)

Base call quality data from DBCLS SRA