|
Status |
Public on Jul 15, 2019 |
Title |
TSC Input control |
Sample type |
SRA |
|
|
Source name |
TS_input
|
Organism |
Mus musculus |
Characteristics |
cell line: F4 cell type: Trophoblast stem cells (TSCs) chip antibody: None
|
Treatment protocol |
trophoblast stem cells were fixed with formaldehyde, lysed and then sonicated with a Misonix Sonicator 3000.
|
Growth protocol |
TS cells were maintained in RPMI1640 (Sigma) supplemented with 20% FBS (Life Technologies), 1mM sodium pyruvate (Life Technologies), 50U/ml penicillin, 50μg/ml streptomycin, 100mM 2-mercaptoethanol (Sigma), 2mM Glutamax (Life Technologies), 25ng/ml FGF4 (R & D Systems), and 1μg/ml heparin (Sigma), with 70% of the media preconditioned by mitotically inactivated E12.5 embryonic fibroblasts (70CM + F4H medium)
|
Extracted molecule |
genomic DNA |
Extraction protocol |
The lysate is incubated with 15ug anti-Esrrb antibody, ), washed, and the bound chromatin eluted. The eluate was reverse-crosslinked, and treated with proteinase K The ChIP-enriched and corresponding input genomic DNA libraries were prepared using the Illumina Genomic Sample Preparation Kit (Illumina) according to the manufacturer’s instruction
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
FASTQ sequences were aligned to the mm9 genome using Bowtie2 v.2.2.3 Peak-calling was performed on the ChIP-Seq library using MACS v.2.2.1, using the following parameters (-g mm -q 0.01) Genome_build: mm9 Supplementary_files_format_and_content: NarrowPeak (BED) file generated by MACS peakcalling
|
|
|
Submission date |
Dec 05, 2018 |
Last update date |
Jul 15, 2019 |
Contact name |
Eiichi Okamura |
E-mail(s) |
eiokamu@gmail.com
|
Organization name |
Shiga University of Medical Science
|
Department |
Research Center for Animal Life Science
|
Lab |
Department of Stem Cells and Human Disease Models
|
Street address |
Seta, Tsukinowa-cho
|
City |
Otsu |
State/province |
Shiga |
ZIP/Postal code |
520-2192 |
Country |
Japan |
|
|
Platform ID |
GPL13112 |
Series (2) |
GSE123361 |
Esrrb function in the extraembryonic ectoderm is required for proper primordial germ cell specification [ChIP-seq] |
GSE123363 |
Esrrb function is required for proper primordial germ cell development in presomite stage mouse embryos |
|
Relations |
BioSample |
SAMN10523697 |
SRA |
SRX5097635 |