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Series GSE104152 Query DataSets for GSE104152
Status Public on May 31, 2018
Title Quantitative proteomic characterization and comparison of T helper 17 and iTreg cells
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Using mass spectrometry-based label-free quantitative (LFQ) proteomics analysis of in vitro differentiated murine Th17 and induced T regulatory (iTreg) cells. More than 4000 proteins covering almost all subcellular compartments were detected. Quantitative comparison of the protein expression profiles resulted in the identification of proteins specifically expressed in the Th17 and iTreg cells. Importantly, our combined analysis of proteome and gene expression data revealed protein expression changes that were not associated with changes at the transcriptional level.
 
Overall design Naïve CD4+ T cells were isolated from 8–10-week-old C57BL/6 mice spleens. Cells were polarized to Th0, Th17 and iTreg conditions for three days. Four biological replicates were prepared for RNA-seq.
 
Contributor(s) Zhi C, Harri L, Imran M, Kari N, Inna S, Anne R, David G, Santosh D B, Robert M
Citation(s) 29851958
Submission date Sep 22, 2017
Last update date May 15, 2019
Contact name Imran Ahammad Mohammad
E-mail(s) imrmoh@utu.fi
Organization name Turku center for Biotechnology
Department Lymphocytes and Inflammation
Lab Chen,Zhi
Street address Tykistokatu 6
City Turku
State/province Finland
ZIP/Postal code 20540
Country Finland
 
Platforms (1)
GPL13112 Illumina HiSeq 2000 (Mus musculus)
Samples (12)
GSM2790851 Exp1_Th0
GSM2790852 Exp1_Treg
GSM2790853 Exp1_Th17
Relations
BioProject PRJNA411825
SRA SRP118695

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
GSE104152_Th17_vs_Th0.txt.gz 858.1 Kb (ftp)(http) TXT
GSE104152_iTreg_vs_Th0.txt.gz 856.7 Kb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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