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Sample GSM3193375 Query DataSets for GSM3193375
Status Public on Dec 18, 2018
Title NonstimulatedSmad4IPA
Sample type SRA
 
Source name MS1 Cell line
Organism Mus musculus
Characteristics stimulation: No
antibody for ip: SMAD4 (Cell Signaling)
cell line: MS1
Treatment protocol Cells were serum starved for 24 hours before addition of fresh media or 1 ng/mL BMP9/10 recombinant protein
Growth protocol Cells were grown in DMEM with 10% FBS and 1% antibiotics/antimycotics.
Extracted molecule genomic DNA
Extraction protocol ChIP was performed using Cell Signaling SimpleChIP Plus Sonication Kit and Smad4 antibody (Cell Signaling 46535).
TruSeq ChIP Library Preparation Kit (Illumina IP-202-1012)
10 ng starting material was used for library prep. DNA quantity was measured using Qubit DNA HS kit (Thermo 32851). Libraries were sequenced using NextSeq 500 High Output v2 kit. Library quality and quantity was assessed using Agilent DNA 1000 chip (Agilent 5067-1504) and Qubit DNA HS kit respectively
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina NextSeq 500
 
Description Smad4 bound DNA from unstimulated Ms1
UnstimUn_peaks.xls
Data processing ChIP-Seq App on Illuminia BaseSpace: MACS2 to identify enriched regions and HOMER for motif discovery
Genome_build: mm10
Supplementary_files_format_and_content: MACS2-peaks
 
Submission date Jun 18, 2018
Last update date Dec 18, 2018
Contact name Stryder Meadows
E-mail(s) smeadows@tulane.edu
Organization name Tulane University
Department Cell and Molecular Biology
Street address 6400 Freret
City New Orleans
State/province LA
ZIP/Postal code 70118
Country USA
 
Platform ID GPL19057
Series (1)
GSE115921 ChIP-Seq: Unstimulated and BMP9/10 Stimulated Endothelial Cells
Relations
BioSample SAMN09435857
SRA SRX4225885

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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