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Series GSE203063 Query DataSets for GSE203063
Status Public on Jul 19, 2022
Title ChIP-seq to reveal the genomic binding landscape of Smad3 in renal tubular cells TCMK1
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Smad3 is an important downstream transcriptional factor of TGF-β signaling in the pathogenesis of renal fibrosis. Understanding the target genes is essential to decode the mechanism underlying Smad3-regulated renal fibrosis. To uncover the potential target genes of Smad3 in renal tubular cells, we applied the ChIP-seq technology to analyze the genomic chromatin binding landscape of Smad3 in TCMK-1 cells. The TCMK-1 cells of 90% confluence were starved in low-serum (0.5% FBS) medium for 6 h followed by stimulation with 5 ng/ml TGF-β1 for 30 min. The cells were harvested for ChIP assay. The precipitated chromatin was used for DNA isolation and deep-sequencing.
 
Overall design ChIP-seq for Smad3 in TGF-β1-stimulated renal tubular cell TCMK-1.
 
Contributor(s) Wang H, Wang L, Peng Z, Li Y
Citation(s) 36091385
Submission date May 15, 2022
Last update date Oct 20, 2022
Contact name Honglian Wang
E-mail(s) honglianwang@swmu.edu.cn
Phone +8615108472354
Organization name the Affiliated Traditional Medicine Hospital of Southwest Medical University
Department Research Center for Integrative Medicine
Lab Research Center for Integrative Medicine
Street address No. 182, Chunhui Road, Longmatan District
City Luzhou
State/province Sichuan
ZIP/Postal code 646000
Country China
 
Platforms (1)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (1)
GSM6153188 TCMK1, TGF-β1 30 min
Relations
BioProject PRJNA838379

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Supplementary file Size Download File type/resource
GSE203063_RAW.tar 376.7 Mb (http)(custom) TAR (of BW)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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