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Series GSE165086 Query DataSets for GSE165086
Status Public on Jan 21, 2021
Title ChIP-seq of Runx2-FLAG in primary chondrocytes.
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Purpose: To demonstrate the role of Transcription factor Runx2 in primary chondrocytes with or without IL-1beta. Method: Fragmented DNA samples were collected from primary chondrocytes of 5-day-old Runx2-Biotin-FLAG-tag mice, cultured with or without IL-1beta. Results: More than 20,000 and 10,000 peaks were gained from chondrocytes without and with IL-1beta, resepectively. Conclusions: Runx2 are associated cellular process and extracellular matrics transcription in primary chondrocytes.
 
Overall design DNA fragment gathered by Anti-Flag antibody or Anti-IgG antibody from primary chondrocytes of 5-day old Runx2-Biotin-FLAG-tag mice.
 
Contributor(s) Nagata K, Saito T
Citation(s) 36261443
Submission date Jan 19, 2021
Last update date Oct 31, 2022
Contact name Kosei Nagata
E-mail(s) knagata-tky@umin.ac.jp
Organization name the University of Tokyo
Department Graduate School of Medicine
Lab Sensory and Motor System Medicine
Street address Hongo7-3-1
City Bunkyo-ku
State/province Tokyo
ZIP/Postal code 113-8655
Country Japan
 
Platforms (1)
GPL13112 Illumina HiSeq 2000 (Mus musculus)
Samples (6)
GSM5025855 Runx2-FLAG
GSM5025856 Runx2-IgG
GSM5025857 Runx2-input
Relations
BioProject PRJNA693553
SRA SRP302586

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE165086_Runx2NearestgenesPeakCallingRunx2_FLAGbyRunx2_input.xlsx 209.6 Kb (ftp)(http) XLSX
GSE165086_Runx2NearestgenesPeakCallinginfR2FLAGbyinfinput.xlsx 221.4 Kb (ftp)(http) XLSX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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