Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Histone
Antigen
H3K27me3

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
p53R248W/+_Lin-Kit+ cells
strain background
C57BL/6
genotype/variation
p53R248W/+
cell type
Hematopoietic stem and progenitor cells
cell subtype
Lin-Kit+ cells
chip antibody
H3K27me3 (clone: 39155, Active Motif)

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Lin-Kit+ cells were fixed with 1% formaldehyde for 15 min and quenched with 0.125 M glycine. Chromatin was isolated by the addition of lysis buffer, followed by disruption with a Dounce homogenizer. Lysates were sonicated and the DNA sheared to an average length of 300-500 bp. Genomic DNA (Input) was prepared by treating aliquots of chromatin with RNase, proteinase K and heat for de-crosslinking, followed by ethanol precipitation. Pellets were resuspended and the resulting DNA was quantified on a NanoDrop spectrophotometer.. For ChIP-seq, Illumina sequencing libraries were prepared from the ChIP and Input DNAs by the standard consecutive enzymatic steps of end-polishing, dA-addition, and adaptor ligation. After a final PCR amplification step, the resulting DNA libraries were quantified and sequenced on Illumina's NextSeq 500 (75 nt reads, single end). Clontech SMART-Seq v4 Ultra Low Input RNA Kit was used for preparing the RNA-seq libraries.

Sequencing Platform

instrument_model
NextSeq 500

mm10

Number of total reads
28776389
Reads aligned (%)
65.8
Duplicates removed (%)
10.3
Number of peaks
7250 (qval < 1E-05)

mm9

Number of total reads
28776389
Reads aligned (%)
65.8
Duplicates removed (%)
10.4
Number of peaks
7238 (qval < 1E-05)

Base call quality data from DBCLS SRA