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Sample GSM289102 Query DataSets for GSM289102
Status Public on Mar 31, 2009
Title NPC_corticosterone_2
Sample type RNA
 
Source name NPC treated with 1 uM corticosterone for 48 hr
Organism Rattus norvegicus
Characteristics Wister
NPC from cerebral cortices of embryo at E15.5
Treatment protocol Cells were treated with 1 uM corticosterone or vehicle (DMSO) for 48 hr.
Growth protocol Neuronal progenitor cells were prepared from cerebral cortices of rat embryo at E15.5. Cells were cultured with 20 ng/ml bFGF on fibronectin coated dish.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using TRIzol reagent (Invitrogen). Quality of the RNA was certificated using Agilent 2100 Bioanalyzer (Agilent Technlogies).
Label biotin
Label protocol cDNA were synthesized by GeneChip T7-Oligo(dT) Promoter Primer Kit(Affymetrix) and TaKaRa cDNA Synthesis Kit (TaKaRa Bio) from 3ug total RNA. Biotinylated cRNA were synthesized by IVT Labeling Kit (Affymetrix) .
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Rat Genome 230 2.0 Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using GeneChip Scanner 3000 7G.
Description gene expression data from rat NPC treated with corticosterone
Data processing Single Array Analysis were calculated by Microarray Suite version 5.0 (MAS5.0) with Affymetrix default setting and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 500.
 
Submission date May 16, 2008
Last update date Dec 24, 2008
Contact name Taira Mayanagi
E-mail(s) taira@nbiochem.med.osaka-u.ac.jp
Organization name Osaka University Graduate School of Medicine
Street address Yamadaoka 2-2
City Suita
State/province Osaka
ZIP/Postal code 565-0871
Country Japan
 
Platform ID GPL1355
Series (1)
GSE11478 Effect of corticosterone treatment on rat neuronal progenitor cells

Data table header descriptions
ID_REF
VALUE Signal
ABS_CALL indicating whether the transcript was present (P), absent (A), or marginal (M)
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 425.45 P 0.000296708
AFFX-BioB-M_at 566.566 P 4.42873e-05
AFFX-BioB-3_at 366.227 P 5.16732e-05
AFFX-BioC-5_at 474.696 P 8.14279e-05
AFFX-BioC-3_at 433.578 P 4.42873e-05
AFFX-BioDn-5_at 2999.75 P 8.14279e-05
AFFX-BioDn-3_at 5093.62 P 7.00668e-05
AFFX-CreX-5_at 15399.8 P 5.16732e-05
AFFX-CreX-3_at 18086.1 P 4.42873e-05
AFFX-DapX-5_at 6.17998 A 0.327079
AFFX-DapX-M_at 12.5066 A 0.327079
AFFX-DapX-3_at 2.26834 A 0.897835
AFFX-LysX-5_at 6.57363 A 0.340661
AFFX-LysX-M_at 14.1816 A 0.544587
AFFX-LysX-3_at 9.25012 M 0.0629293
AFFX-PheX-5_at 1.60745 A 0.941556
AFFX-PheX-M_at 1.14903 A 0.973889
AFFX-PheX-3_at 26.0737 A 0.41138
AFFX-ThrX-5_at 15.4921 A 0.227617
AFFX-ThrX-M_at 4.80295 A 0.559354

Total number of rows: 31099

Table truncated, full table size 954 Kbytes.




Supplementary file Size Download File type/resource
GSM289102.CEL.gz 2.6 Mb (ftp)(http) CEL
GSM289102.CHP.gz 165.8 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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