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Sample GSM572203 Query DataSets for GSM572203
Status Public on Dec 31, 2013
Title Cortex-Sham-8h-Rep1
Sample type RNA
 
Source name Infarct Cortex
Organism Mus musculus
Characteristics strain: C57/Bl6
age: 8 days
treatment: Ctrl
time point: 8h
tissue: brain cortex
Treatment protocol Pups were anesthetized with 1.5% isoflurane in 30% O2/70% N2 mixture and underwent unilateral HI. The right common carotid artery was exposed through a ventral midline neck incision and permanently occluded by electrocoagulation (Aaron Medical Industries Inc, Florida, USA), where the occlusion was verified The wound was sutured and mouse pups were returned to their mother for 1.5–2 h. Sham control rats (n = 4) underwent the identical procedure, without carotid artery occlusion. Pups were then placed in an 8% O2/92% N2 humidified chamber at 37°C for 1 h. This combined procedure results in select neuronal damage or infarction in the hemisphere ipsilateral to the carotid occlusion, whereas hypoxia alone (contralateral hemisphere) does not produce any significant brain injury (reference). Following the HI or sham surgery procedure, all pups were returned to their dam and kept under standard housing conditions for the remainder of the study.
Growth protocol All animal work conducted in this study was approved by the University of New South Wales (UNSW) Animal Ethics and Experimentation Committee and performed in accordance with the guidelines of the National Health and Medical Research Council (Australia). C57 Black 6 mouse pups were obtained from Animal Resources Centre (Perth, WA) and were housed under standard housing conditions in the UNSW Biological Resources Centre animal facility throughout experiments.
Extracted molecule total RNA
Extraction protocol RNA was extracted and cleaned up with QIAGEN miRNeasy mini kit in accordance with the prescribed protocol provided with the kit. Quality control was performed with E-gene HDA-GT12 genetic analyzer.
Label biotin
Label protocol Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays
 
Hybridization protocol Standard Illumina hybridization protocol with a hybridization duration of 17h.
Scan protocol Standard Illumina scanning protocol with a pmt value=478
Description Replicate 1
4514990159_E
Data processing The data were normalised using median normalisation with GeneSpring Ver 7.3
 
Submission date Jul 29, 2010
Last update date Dec 31, 2013
Contact name Minghui Jessica Chen
Organization name Menzies Research Institute
Department Neuroscience group
Lab A/P Steve Cheung
Street address Menzies Research Institute, University of Tasmania, Private Bag 24
City Hobart
State/province Tasmania
ZIP/Postal code 7001
Country Australia
 
Platform ID GPL6885
Series (2)
GSE23317 Global transcriptomic profiling of hypoxic ischemia in an in vivo neonatal mouse model: cortex
GSE23333 Global transcriptomic profiling of hypoxic ischemia in an in vivo neonatal mouse model

Data table header descriptions
ID_REF
VALUE Median normalisation

Data table
ID_REF VALUE
ILMN_1248788 0.6179903
ILMN_2707227 0.8921049
ILMN_2896528 0.747618
ILMN_2721178 0.75239915
ILMN_1227723 0.83769786
ILMN_3033922 0.91640717
ILMN_3092673 0.82201856
ILMN_2730714 0.7827359
ILMN_3162224 0.9217338
ILMN_2816356 1.0360416
ILMN_2808939 0.93078864
ILMN_2634564 0.773753
ILMN_1216623 0.7488974
ILMN_1215157 0.7355313
ILMN_1228777 1.0524763
ILMN_2737647 0.9879318
ILMN_1216425 1.1005527
ILMN_2734484 0.8105925
ILMN_2652961 0.9701661
ILMN_2952292 0.91565657

Total number of rows: 25697

Table truncated, full table size 578 Kbytes.




Supplementary data files not provided
Raw data are available on Series record
Processed data included within Sample table
Processed data are available on Series record

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