|
Status |
Public on Jul 08, 2020 |
Title |
H3K4me3_LPS_24h |
Sample type |
SRA |
|
|
Source name |
Bone marrow-derived macrophage
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6 chip antibody: H3K4me3 (Active Motif, 39159) treatment: LPS 24h
|
Treatment protocol |
For LPS treatment, 100 ng/ml of LPS (Sigma-Aldrich) was added to the medium.
|
Growth protocol |
Bone marrow cells were flushed from femurs and tibias of male mice between 6 and 9 weeks of age, and were grown in DMEM/F12 (Thermo Fisher) supplemented with 10% FBS (HyClone), 1% penicillin–streptomycin (Thermo Fisher), 1% l-glutamine (Thermo Fisher), and 40 ng/ml of recombinant mouse M-CSF (576406; BioLegend) for 7-8 days. The medium was changed every 3 days. Differentiated BMDMs were detached from plates using StemPro Accutase Cell Dissociation Reagent (Thermo Fisher) and replated into 12-well tissue culture dishes at a density of 5 x 105 cells per well prior to cell stimulation.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
ChIP-seq libraries were prepared using a TruSeq ChIP Library Preparation kit (Illumina) according to the manufacturer’s protocol.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina Genome Analyzer IIx |
|
|
Data processing |
ChIP-seq reads were aligned to the mm9 genome assembly using STAR aligner. Genome_build: mm9 Supplementary_files_format_and_content: bedGraph files were generated using Homer.
|
|
|
Submission date |
Apr 17, 2019 |
Last update date |
Jul 08, 2020 |
Contact name |
Ichiro Manabe |
E-mail(s) |
manabe-tky@umin.ac.jp
|
Organization name |
Chiba University
|
Street address |
1-8-1 Inohana, Chuo
|
City |
Chiba |
ZIP/Postal code |
260-8670 |
Country |
Japan |
|
|
Platform ID |
GPL11002 |
Series (2) |
GSE129963 |
ChIP-seq profiling of macropahge response to LPS |
GSE130056 |
Analysis of long noncoding RNAs in macrophages |
|
Relations |
BioSample |
SAMN11457145 |
SRA |
SRX5705700 |