Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Histone
Antigen
H3K27ac

Cell type

Cell type Class
Blood
Cell type
MOLT-16
Primary Tissue
Blood
Tissue Diagnosis
Leukemia

Attributes by original data submitter

Sample

source_name
MOLT16 cell line DSMZ Acc 29
antibody
H3K27ac (Abcam, ab4729)
sorted cells
CD2 +, CD3 +, CD4 -, CD5 +, CD6 +, CD7 +, CD8 -, CD13 -, CD19 -, CD34 -, TCRalpha/beta +, TCRgamma/delta -
sample type
human near diploid karyotype - 46(43-47)<2n>XX, t(3;11)(p21;p13), t(8;14)(q24;q11) - t(8;14)(q24;q11) and 11p13 breakpoint

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
2x10^7 cells crosslinked with methanol-free formaldehyde (1% final concentration) RT for 7 min, reaction quenched with glycine . Nuclei isolation performed using truChIP Chromatin Shearing Reagent KIT (Covaris, PN520154). Purified chromatin fragmented by sonication (Covaris, M220, Focused-ultrasonicator). Chromatin fraction ON IP incubation with 40 μl of Protein A UltraLink™ Resin (Thermo-Scientific, 53139) and 4 μg Anti-Histone H3 (acetyl K27) antibody - ChIP Grade (Abcam, ab4729). Day after, bead wash and ON reverse cross-linking by incubation at 65 °C. Input sample was also included (from 1.6x10^6 cells). DNA purified by Chromatin IP DNA Purification Kit (Active-Motif, 58002). library prepared using NEBNext Ultra DNA library Prep Kit (New England Biolabs,E73370S) and sequenced by NextSeq 500 (Illumina). DNA fragmentation, End repair, 5' Phosphorilation, dA-Tailing, Adaptor Ligation with U Excision, Size selection/CleanUp, PCR enrichment, Final CleanUp

Sequencing Platform

instrument_model
NextSeq 500

hg38

Number of total reads
32275619
Reads aligned (%)
98.5
Duplicates removed (%)
4.5
Number of peaks
11836 (qval < 1E-05)

hg19

Number of total reads
32275619
Reads aligned (%)
97.5
Duplicates removed (%)
6.0
Number of peaks
11657 (qval < 1E-05)

Base call quality data from DBCLS SRA