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Sample GSM642802 Query DataSets for GSM642802
Status Public on Nov 21, 2011
Title TES Control 4 4h
Sample type RNA
 
Source name retina
Organism Rattus norvegicus
Characteristics strain: Brown Norway Rat
gender: male
age: 8 weeks
Extracted molecule total RNA
Extraction protocol mRNA of retina was isolated 4h after transcornial electrical stimulation and compared to sham animals using RNAeasy Isolation Kit (Ambion, Austin, Texas, USA) according to manufacturers instructions.
Label Biotin
Label protocol Three microliter total RNA was used for each sample to obtain linearly amplified labeled cRNA by using GeneChip® One-Cycle Target Labeling kit (Affymetrix, Santa Clara, CA, USA) as described by manufacturer. Briefly, total RNA was used to generate double-stranded cDNA with the T7-oligo (dT) primer. This double-stranded cDNA was used in vitro transcription and biotin labeling steps. Labeled cRNA yield and purity were determined by measuring the absorbance at 260 and 280nm. All the cRNA 260/280 ratios were between 1.9 and 2.1. Quality control of the labeled cRNA products was assessed by performing 1µg labeled cRNA on 2% agarose gel to see similar RNA smear type.
 
Hybridization protocol 15 micrograms of labeled cRNA from retina was fragmented, and 10ug was hybridized to Affymetrix Rat Gene 1.0 ST Gene Chip arrays for 18-24h (Affymetrix Inc.). Gene chip was washed and stained with streptavidin-phycoerythrin.
Scan protocol The chip was scanned at 6um resolution with Agilant model G2500A Gene Array scanner. A visual quality control measurement was performed to ensure proper hybridization after each chip was scanned.
Data processing For statistical analysis of microarray data all .cel files were imported to GeneSpring GX software (Agilent Technologies Inc.) where GC-RMA algorithm was applied to yield log signal values on each probe set. All transcripts with a minimum change of 1.2 fold together with a p value less than 0.05 were selected using Significance Analysis of Microarray (SAM) (Tusher VG, 2001).
 
Submission date Dec 20, 2010
Last update date Nov 21, 2011
Contact name Gabriel Willmann
E-mail(s) Gabriel.Willmann@med.uni-tuebingen.de
Organization name University Eye Hospital and Centre for Ophthalmology Tübingen
Street address Schleichstrasse 12-16
City Tübingen
ZIP/Postal code 72076
Country Germany
 
Platform ID GPL10741
Series (1)
GSE26174 Gene Expression Profiling of the Retina after Transcorneal Electrical Stimulation in Wildtype Brown Norway Rats

Data table header descriptions
ID_REF
VALUE log2 RMA signal
DETECTION P-VALUE Significance value

Data table
ID_REF VALUE DETECTION P-VALUE
10700001 10.376 0
10700002 2.64945 0.334427
10700003 8.8796 0
10700004 2.02624 0
10700005 8.40156 2.99022e-32
10700006 1.51983 0.779934
10700007 1.72027 0.297453
10700008 1.64314 0.343891
10700009 4.75928 0.763464
10700010 1.80836 0.8837
10700011 2.05511 0.949155
10700012 1.96545 0.944369
10700013 10.066 2.33826e-36
10700014 9.21869 7.05046e-34
10700015 4.96336 0.355408
10700016 1.58103 0.522485
10700017 2.38292 0.254392
10700018 1.47018 0.68108
10700019 1.60123 0.925865
10700020 11.0188 1.17826e-36

Total number of rows: 213067

Table truncated, full table size 5730 Kbytes.




Supplementary file Size Download File type/resource
GSM642802_I9R_047c04.CEL.gz 4.3 Mb (ftp)(http) CEL
GSM642802_I9R_047c04.rma_exon_default_dabg.chp.gz 1.9 Mb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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