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Sample GSM911917 Query DataSets for GSM911917
Status Public on Dec 24, 2013
Title whole_ctrl_1
Sample type RNA
 
Source name whole kidneys
Organism Rattus norvegicus
Characteristics gender: male
strain: Wistar/ST
age: 8 weeks old
tissue: whole kidneys
agent: vehicle
dose: control
Treatment protocol Cisplatin (0.5 mg/mL; Randa®; Nippon Kayaku Co. Ltd., Tokyo, Japan) was administered intraperitoneally; the same volume of saline solution was injected in the sham controls.
Growth protocol Male Wistar/ST rats (8 weeks old) were purchased from SLC Animal Research Laboratories (Shizuoka, Japan). The rats were fed normal pellet food ad libitum, and given water freely.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with the RNeasy Mini Kit (Qiagen GmbH, Hilden, Germany)
Label Digoxigenin-UTP
Label protocol Digoxigenin (DIG)-labeled cRNA was generated from total RNA extracted from the proximal tubules or whole kidney using Applied Biosystems Chemiluminescent Reverse Transcription-In Vitro Transcription (RT-IVT) Labeling Kit v2.0 (Applied Biosystems part of Life Technologies, Foster City, CA, USA)
 
Hybridization protocol A total of 10 μg of labeled cRNA from each RT-IVT reaction was hybridized onto Rat Genome Survey Microarray at 55°C for 16 h.
Scan protocol Microarrays were analyzed using the ABI 1700 Chemiluminescent Microarray Analyzer (Applied Biosystems)
Description Rat Genome Survey Microarray® (Applied Biosystems)
Data processing The array contained 34,656 oligonucleotide probes, including 26,857 individual gene probes and more than 1000 control probes. Microarray signal data were analyzed using Spotfire® software (TIBCO Software Inc. Palo Alto, CA). Expression values were normalized across the experiments with each 50% percentile values. Genes were defined as detectable on the basis of the recommendations from Applied Biosystems; a gene with a signal:noise ratio > 3.0 in 2 or 3 assays, and a FLAG value < 5000 was considered to be detectable. Normalized signal data were analyzed statistically with a one-way ANOVA. Probability values of less than 0.05 were considered statistically significant.
 
Submission date Apr 10, 2012
Last update date Dec 24, 2013
Contact name Satohiro Masuda
E-mail(s) masuda@kuhp.kyoto-u.ac.jp
Phone +81-75-751-3586
Fax +81-75-751-3586
Organization name Kyoto University Hospital
Department Pharmacy
Lab Masuda
Street address Shogoin
City Kyoto
ZIP/Postal code 606-8507
Country Japan
 
Platform ID GPL2996
Series (1)
GSE37133 Gene expression profiles in isolated proximal tubules and whole kidneys of rats after cisplatin-administration

Data table header descriptions
ID_REF
VALUE Expression values were normalized across the experiments with each 50% percentile values

Data table
ID_REF VALUE
20693655 2.587318553
20695021 8.479032239
20697227 8.032225098
20698369 6.700227328
20698782 2.319631007
20701664 42.79742934
20703606 18.37338043
20704144 2.949230246
20704436 0.940770263
20707360 3.252068136
20707856 23.40357142
20708360 6.281015033
20708437 3.858495647
20708753 59.05264668
20711332 5.736527938
20711520 2.884208047
20712530 3.725749057
20713554 14.11663456
20713880 15.7052657
20714771 4.613459062

Total number of rows: 1219

Table truncated, full table size 24 Kbytes.




Supplementary file Size Download File type/resource
GSM911917_whole_ctrl_1.txt.gz 241.7 Kb (ftp)(http) TXT
Processed data included within Sample table

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