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Sample GSM591749 Query DataSets for GSM591749
Status Public on Dec 07, 2010
Title brain_at 48h after trauma_rep2
Sample type RNA
 
Source name lateral cortex, traumatic brain injury
Organism Rattus norvegicus
Characteristics strain: Wistar
gender: male
age: 8 weeks old
tissue: brain, lateral cortex
stress: moderate fluid percussion injury
time: 48h
Treatment protocol Rats were transcardially perfused with physiological saline under general anesthesia at 3, 6, 12 and 48 h after moderate fluid percussion or the sham operation. The brains were quickly removed and cut coronally into 2-mm-thick sections. The cortices that corresponded to the contusion areas were removed. They were then placed in RNAlaterTM (Takara, Japan) overnight at 4°C and stored at –20 °C until use.
Growth protocol Rats were performed craniectomy of diameter 4.8 mm over the right parietal cortex under general anesthesia. A cranial Leur adapter of inner diameter 2.5 mm was placed on the craniectomy site and mounted to the skull by using dental acrylic resin. The animals were housed for 48 h, and they were then re-anesthetized. The cranial Leur adapter was filled with saline and attached to the fluid percussion device. Animals were subjected to sham or moderate (3.3 ± 0.3 atm) fluid percussions.
Extracted molecule polyA RNA
Extraction protocol Polyadenylated RNA was isolated using the Quickprep micro mRNA purification kit (Amersham, USA) according to the manufacturer’s protocol.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the Affymetrix protocol from 0.4 ug PolyA RNA (One-cycle Target Labeling: GeneChip Expression Analysis Technical Manual, 701021 Rev. 5).
 
Hybridization protocol cRNA were hybridized on GeneChip rat genome 230 2.0 using the Hybridization Oven 640 110V. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the GeneChip Scanner 3000 (Affymetrix 00-0074).
Description impacted region
48(M-23)
Data processing Data were pre-processed by RMA method, filtered, and normalized using the GeneSpring GX v11.0.2 software (Agilent). Compared data from experimental conditions are normalized versus array's base line median considered for each case.
 
Submission date Sep 09, 2010
Last update date Dec 07, 2010
Contact name Hideki Shojo
E-mail(s) [email protected]
Phone 81-55-273-9546
Fax 81-55-273-6753
Organization name University of Yamanashi
Department Graduate School of Medical Science
Lab Department of Legal Medicine
Street address 1110 shimokato
City Chuo
State/province Yamanashi
ZIP/Postal code 409-3898
Country Japan
 
Platform ID GPL1355
Series (1)
GSE24047 Gene expression profiles after traumatic brain injury

Data table header descriptions
ID_REF
VALUE log2 RMA signal divided by median of all samples

Data table
ID_REF VALUE
AFFX-BioB-5_at -0.19
AFFX-BioB-M_at -0.18
AFFX-BioB-3_at -0.18
AFFX-BioC-5_at -0.19
AFFX-BioC-3_at -0.17
AFFX-BioDn-5_at -0.20
AFFX-BioDn-3_at -0.06
AFFX-CreX-5_at -0.07
AFFX-CreX-3_at -0.08
AFFX-DapX-5_at -0.01
AFFX-DapX-M_at 0.00
AFFX-DapX-3_at 0.03
AFFX-LysX-5_at -0.13
AFFX-LysX-M_at -0.15
AFFX-LysX-3_at -0.02
AFFX-PheX-5_at -0.01
AFFX-PheX-M_at 0.01
AFFX-PheX-3_at -0.01
AFFX-ThrX-5_at 0.00
AFFX-ThrX-M_at 0.00

Total number of rows: 31099

Table truncated, full table size 505 Kbytes.




Supplementary file Size Download File type/resource
GSM591749.CEL.gz 4.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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