Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Unclassified
Antigen
Unclassified

Cell type

Cell type Class
Blood
Cell type
Natural Killer T-Cells
MeSH Description
A specific natural killer T-cell subtype that expresses an invariant T-cell receptor alpha-chain.

Attributes by original data submitter

Sample

source_name
sorted cells from thymus
strain
L-DKO mice (deficient in Id2 and Id3)
age
3-5 weeks
tissue
thymus
cell type
Invariant Natural Killer T (iNKT) cells
sorting strategy
CD1dTet+ TCRβ+
molecule subtype
genomic DNA + crosslinked, bound protein

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Thymii were harvested from mice, and thymocytes were stained with appropriate antibodies for sorting. Following sort, Cells were fixed for 15 min in PBS containing 1.5 mM EGS(ethylene glycol-bis(succinic acid N-hydroxysuccinimide ester)), followed by incubation for 15 min with 1% formaldehyde. Formaldehyde was quenched by incubation for 10 min with 0.2 M glycine, and then washed twice with PBS and pellets were frozen in liquid nitrogen. Crosslinked cells were lysed, washed and sonicated for 22 cycles using a Biorupter Plus sonicator. Lysates were cleared with dilution buffer, and incubated overnight at 4°C with magnetic beads bound with 15 μg of anti-E2A antibody (V-18, Santa Cruz Biotechnology, Lot G0814) or 3 μl anti-H3K4me2 antibody (Millipore, 07-030, Lot 2430486). Beads were washed multiple times with appropriate buffers. Bound complexes were then eluted from beads by incubation for 30 min at 65 °C with shaking in elution buffer. Crosslinks were reversed by incubation overnight at 65°C. RNA and proteins were digested, followed by DNA purification using a ChIP DNA Clean and Concentrator kit (Zymoresearch). Libraries were prepared with the NEBNext primer set which involved applying ChIP DNA to end repair, A-tailing, adapter ligation, PCR amplification. They were then cleaned and size selected by AMPure beads (Agencourt)

Sequencing Platform

instrument_model
Illumina HiSeq 4000

mm10

Number of total reads
55354309
Reads aligned (%)
78.6
Duplicates removed (%)
11.2
Number of peaks
2450 (qval < 1E-05)

mm9

Number of total reads
55354309
Reads aligned (%)
78.5
Duplicates removed (%)
11.2
Number of peaks
2532 (qval < 1E-05)

Base call quality data from DBCLS SRA