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Sample GSM3502115 Query DataSets for GSM3502115
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

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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