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Sample GSM563242 Query DataSets for GSM563242
Status Public on Feb 01, 2011
Title Epilepsy patient E3, 2 hours GC treatment
Sample type RNA
 
Source name Mononuclear cells, epilepsy patient E3, 2 hours after GC administration
Organism Homo sapiens
Characteristics tissue: peripheral blood
cell type: mononuclear cells
disease state: epilepsy, non-leukemic
treatment: dexamethasone
treatment_time: 2 hrs
patient: E3
Treatment protocol Single administration of the glucocorticoid dexamethasone (20 mg/m2).
Growth protocol None.
Extracted molecule total RNA
Extraction protocol For total RNA isolation, TRIreagent (MRC Inc., Cincinnati, OH, USA) was used according to the manufacturer’s protocol. Briefly, mononuclear cells isolated from peripheral blood (Lymphoprep) were lysed with TRIreagent, 200ul of chloroform was added, the mixture was centrifuged, and the RNA from the aqueous phase was precipitated with isopropanol. The pelleted RNA was washed in 70% ethanol in DEPC-water and resuspended in nuclease-free water. RNA was further processed with the RNeasy Cleanup Kit (Qiagen), and quantity and purity was determined by optical densitiy measurements (OD260/280) and RNA integrity using the 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA,USA). Only high quality RNA was further processed.
Label biotin
Label protocol 1ug total RNA was processed to generate a biotinylated hybridization target using “One Cycle cDNA Synthesis” and “One Cycle Target Labelling” kits from Affymetrix (Affymetrix, Santa Clara, CA). All procedures were performed according to the manufacturer’s protocols.
 
Hybridization protocol 20ug of cRNA were fragmented at 95C using the Affymetrix fragmentation buffer, mixed with hybridization buffer containing hybridization controls and hybridized to Affymetrix HG U133 Plus 2.0 GeneChips.
Scan protocol Fluorescence signals were recorded by an Affymetrix scanner 3000 and image analysis was performed with the GCOS (version 1.4.0.036) software.
Description Gene expression of mononuclear cells isolated from the peripheral blood (using Lymphoprep) of the epilepsy patient E3 taken 2 hours after GC administration.

E3-2h
Data processing The raw data was preprocessed in R (version 2.10) using the GCRMA algorithm (Bioconductor's GCRMA package version 2.18.1).
 
Submission date Jul 06, 2010
Last update date Feb 01, 2011
Contact name Johannes Rainer
E-mail(s) johannes.rainer@eurac.edu
Organization name Eurac Researc
Department Institute for Biomedicine
Lab Biomedical Informatics
Street address Via A. Volta 21
City Bolzano
ZIP/Postal code 39100
Country Italy
 
Platform ID GPL570
Series (1)
GSE22779 Gene expression data of non-leukemic individuals before and during in-vivo glucocorticoid treatment

Data table header descriptions
ID_REF
VALUE GCRMA preprocessed intensity, log2 scale

Data table
ID_REF VALUE
1007_s_at 4.926976394
1053_at 5.348929287
117_at 4.954437397
121_at 3.658210503
1255_g_at 1.503731078
1294_at 6.385323133
1316_at 2.831451589
1320_at 1.899045209
1405_i_at 12.52147374
1431_at 1.921316344
1438_at 2.293020386
1487_at 4.852865023
1494_f_at 2.378834066
1552256_a_at 3.464988547
1552257_a_at 5.745283831
1552258_at 2.920566238
1552261_at 2.317866683
1552263_at 9.074348352
1552264_a_at 8.346176891
1552266_at 1.71281401

Total number of rows: 54675

Table truncated, full table size 1212 Kbytes.




Supplementary file Size Download File type/resource
GSM563242.CEL.gz 4.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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