NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM678387 Query DataSets for GSM678387
Status Public on Feb 23, 2011
Title IM_vehicle_rep2
Sample type RNA
 
Source name Kidney inner medulla collected from vehicle treated control rat
Organism Rattus norvegicus
Characteristics strain: Sprague-Dawley
tissue: kidney inner medulla
gender: male
body weight: 200–250 g
Treatment protocol For vehicle (saline, 1 µl/h, s.c. for 5 d) or dDAVP (40 ng/h, s.c. for 5 d, D5d) infusion, osmotic minipumps were implanted subcutaneously in the neck of each rat. osmotic minipumps were removed from rats under light enflurane inhalation anesthesia and rats were awakened, returned to metabolic cages, and kept for 3hr (D5d-3h).
Growth protocol Pathogen-free male Sprague-Dawley rats were obtained from Charles River. The animal protocols were approved by the Animal Care and Use Committee of Kyungpook National University, and all animal experiments were conducted according to the guidelines of Kyungpook National University. Vehicle-treated control rats and dDAVP-treated rats were maintained in metabolic cages. All animals were maintained on a fixed amount of standard rodent diet (20 g/220 g BW/day) with free access to water intake.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol The Affymetrix GeneChip® procedure for generation of the biotin-labeled single-stranded cDNA by in vitro transcription were performed according to the manufacturer's instructions from 300ng total RNA(GeneChip® Whole Transcript (WT) Sense Target Labeling Assay Rev.5). Protocol performed using the Whole Transcript Sense Target Labeling and Control Reagents (Affymetrix 900652).
 
Hybridization protocol Following fragmentation, 5.5 ug of framented cDNA were hybridized for about 17 hr at 45℃ on Rat Gene 1.0 ST array. The hybridized probe arrays were stained and washed with GeneChip® Hybridization, Wash and Stain Kit using the Fluidics Station 450(Affymetrix).
Scan protocol The stained GeneChips were scanned with a GeneChip® Scanner 3000+ 7G(Affymetrix) a 570 nm.
Description Gene expression data at the control state
Data processing The RMA algorithm was used for expression summary and signal calculation of Affymetrix Rat Gene 1.0 ST array data. Sketch Quantile normalization was performed for the signal normalization.
 
Submission date Feb 22, 2011
Last update date Feb 23, 2011
Contact name Tae-Hwan Kwon
E-mail(s) thkwon@knu.ac.kr
Phone +82 53 420 4825
Fax +82 53 422 1466
Organization name School of Medicine, Kyungpook National University
Department Department of Biochemistry and Cell Biology
Street address Dongin-dong 101
City Taegu
ZIP/Postal code 700-422
Country South Korea
 
Platform ID GPL6247
Series (1)
GSE27449 Changes of mRNA expressin in rat kidney inner medulla in response to dDAVP stimulation/ withdrawal

Data table header descriptions
ID_REF
VALUE RMA signal intensity
ABS_CALL
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
10821838 1488.9027 P 0
10800328 77.96002 P 0
10874458 155.53256 P 0
10834373 122.99212 P 0
10763430 2853.3442 P 0
10883125 636.96094 P 0
10806375 718.96735 P 0
10794685 761.62305 P 0
10781216 129.50627 P 1.00E-05
10773004 85.35466 P 1.00E-05
10919076 122.383 P 0
10850056 153.56909 P 0
10791677 803.98157 P 0
10929562 402.073 P 0
10875245 1796.1432 P 0
10852174 124.88643 P 0
10809457 516.5167 P 0
10933042 364.54224 P 0
10783378 163.29965 P 0
10798513 92.83935 P 0

Total number of rows: 28524

Table truncated, full table size 670 Kbytes.




Supplementary file Size Download File type/resource
GSM678387.CEL.gz 4.1 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap