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Series GSE61983 Query DataSets for GSE61983
Status Public on Nov 01, 2014
Title A combined omics approach to generate the surface protein atlas of human naive CD4+ T cells during early TCR activaion
Organism Homo sapiens
Experiment type Expression profiling by array
Summary To increase the dataset of our proteomic naive CD4+ T cell surface atlas, we applied whole genome microarray expression analysis. The NCBI RefSeq accession number of all transcripts which were detected in naive and stimulated CD4+ T cells (aCD3/aCD28 for 3h) of four different donors, was mapped to the corresponding UniProtKB accession number. For these UniProtKB ACs, we extracted the subcellular localization (UniProt_SL) annotation from the UniProtKB/Swiss-Prot database or if not available the subcellular localization was predicted unsing LocTree3 and PolyPhobius. This led to the identification of 908 genes coding for proteins located on the surface of human naive and/or activated CD4+ T cells.
 
Overall design Gene expression in human naive T cells and naive T cells which were stimulated with aCD3/aCD28 for 3h was measured. Naive T cells from four different human blood donors were analyzed.
 
Contributor(s) Suttner K, Graessel A
Citation(s) 25991687
Submission date Oct 02, 2014
Last update date Oct 11, 2016
Contact name Kathrin Suttner
Organization name ZAUM-Center for Allergy and Environment
Department Helmholtz Zentrum und TU Muenchen
Street address Biedersteiner Str. 29
City Muenchen
ZIP/Postal code 80802
Country Germany
 
Platforms (1)
GPL14550 Agilent-028004 SurePrint G3 Human GE 8x60K Microarray (Probe Name Version)
Samples (8)
GSM1517935 naiveTcells_0h_donor1
GSM1517936 naiveTcells_3h_donor1
GSM1517937 naiveTcells_0h_donor2
Relations
BioProject PRJNA262866

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
GSE61983_RAW.tar 24.9 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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