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Sample GSM3358406 Query DataSets for GSM3358406
Status Public on Aug 29, 2018
Title rat 4, at T0
Sample type RNA
 
Source name Blood
Organism Rattus norvegicus
Characteristics animal: rat 4
gender: male
strain: spontaneously hypertensive rats (SHR)
age: 16 weeks
tissue: Blood
treatment: before MCA occlusion
time: control
Treatment protocol Stroke was induced by thread occlusion of the middle cerebral artery (MCAo) using a silicon-coated thread which was maneuvered through the internal carotid until resistance was felt and a drop in cerebral blood flow noted on Laser Doppler; Whole blood (250µl) was drawn from the lateral tail vein (1ml syringe, 26G needle) into 500 international units of heparin (500IU, Pfizer) at 0 (immediately before anesthesia induction), 1, 2, 3, and 6 hours post MCA occlusion. The 24 hour sample was taken by heart puncture immediately following anesthetic overdose
Growth protocol Eight male 16 week old spontaneously hypertensive rats were maintained under standard housing conditions with a normal light/dark cycle with ad libitum access to normal rat chow and water for two weeks before stroke induction.
Extracted molecule total RNA
Extraction protocol RNA was prepared from the whole blood cell pellets using the PAXgene Blood RNA Kit (PreAnalytiX #762174, Qiagen).
Label biotin
Label protocol The Encore Biotine module (NuGen, San Carlos, CA, USA; cat#4200-12) was used for fragmentation and labelling. Gene hybridisation was performed using the Affymetrix GeneChip Expression 3’ Amplification Reagent Hybridisation Controls kit (Affymetrix, Santa Clara, CA, USA; cat#900454)
 
Hybridization protocol Samples were randomly hybridized to the GeneChip® RatGene 1.0 ST arrays (Affymetrix, Santa Clara CA, USA; cat#9011730).
Scan protocol GeneChips were scanned using the Fluidics control station (Affymetrix GeneChip Fluidics Station 450, Affymetrix, Santa Clara, CA, USA)
Description gene expression data from SHR rat blood before MCA occlusion
Data processing For gene expression, pairwise comparisons were made between neighboring time points of the experiment using linear models, and the resulting F-statistic was used to identify genes whose expression varied the most across the time course of the experiment. Models were constructed, and significance testing was performed using the R package limma
Genes with expression varying the most over time were ranked by p-value of the F statistic, with a cut-off of 5x10^-7
 
Submission date Aug 28, 2018
Last update date Aug 29, 2018
Contact name Marie Dagonnier
E-mail(s) [email protected]
Phone 486145143
Organization name The Florey Institutes for Neurosciences
Department Stroke
Lab Basic Sciences
Street address Place du Fichaux, 38
City Pont-à-Celles
State/province Hainaut
ZIP/Postal code 6230
Country Belgium
 
Platform ID GPL6247
Series (1)
GSE119121 Expression data from blood of rats

Data table header descriptions
ID_REF
VALUE RMA signal

Data table
ID_REF VALUE
10940437 6.695029
10940438 5.915827
10940439 5.187137
10940440 6.926814
10940441 9.415305
10940442 5.137888
10940443 13.05577
10940444 11.1634
10940445 9.980796
10940446 6.598978
10940447 6.242438
10940448 6.757666
10940449 6.772759
10940450 7.695999
10940451 4.440022
10940452 5.710468
10940453 6.370647
10940454 10.11961
10940455 6.536903
10940456 9.602365

Total number of rows: 27596

Table truncated, full table size 482 Kbytes.




Supplementary file Size Download File type/resource
GSM3358406_19_RaGene-1_0-st-v1_.CEL.gz 4.1 Mb (ftp)(http) CEL
Processed data included within Sample table
Processed data are available on Series record

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