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Sample GSM313697 Query DataSets for GSM313697
Status Public on Aug 23, 2008
Title Liver_PB_CAR_rep4
Sample type RNA
 
Channel 1
Source name Liver, phenobarbital-treated
Organism Mus musculus
Characteristics Genetic background: CAR deficient
Strain: C57BL/6J
Gender: male
Age: 9-12 weeks
Tissue: liver
Treatment: 100 mg/kg phenobarbital
Biomaterial provider Viola Tamasi
Treatment protocol Animals were injected i.p. with phenobarbital (100mg/kg). After 12h they were sacrificed.
Growth protocol Animals had free acess to food (standard laboratory chow) and drinking water. They were maintained in 12-hour light/12-hour dark cycle.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using TRIzol reagent (Invitrogen) according to the manufacturer protocol and purified by RNeasy Mini Kit (Qiagen). Spectrofotometer (Nanodrop) was used to monitor the quality of RNA.
Label Cy5
Label protocol Lucidea Universal scorecard (GE Helthcare) was added as an universal reference for microarray experiment. 10 μg of total RNA was used for labeling using Agilent Fluorescent Direct Label Kit (Agilent) according to manufacturer protocol.
 
Channel 2
Source name Liver, untreated CAR pool
Organism Mus musculus
Characteristics Genetic background: CAR deficient
Strain: C57BL/6J
Gender: male
Age: 9-12 weeks
Tissue: liver
Treatment: 5% DMSO in corn oil
Biomaterial provider Viola Tamasi
Treatment protocol Animals were injected i.p. vehicle (5% DMSO in corn oil). After 12h they were sacrificed.
Growth protocol Animals had free acess to food (standard laboratory chow) and drinking water. They were maintained in 12-hour light/12-hour dark cycle.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using TRIzol reagent (Invitrogen) according to the manufacturer protocol and purified by RNeasy Mini Kit (Qiagen). Spectrofotometer (Nanodrop) was used to monitor the quality of RNA. RNAs from 6 replicates were pooled and used for hybridization.
Label Cy3
Label protocol Firefly luciferase (Promega) was added as an universal reference for microarray experiment. 10 μg of total RNA was used for labeling using Agilent Fluorescent Direct Label Kit (Agilent) according to manufacturer protocol.
 
 
Hybridization protocol Sterolgene V1 slides were washed before hybridization at room temperature 5 min in 2xSSC and 0.1%SDS, 3 min in 0.2xSSC and 2 min in MilliQ water and dried by centrifugation. Samples were denatured and hybridized in 3xSSC and 0.2% SDS hybridization buffer at 65˚C for 16 hours using humidified hybridization chambers (HybChambers, GeneMachines). After hybridizations slides were washed at room temperature for 5 min in 2xSSC and 0.5% SDS, followed by 5 min in 0.5xSSC, then 5 min in 0.05xSSC and dried by centrifugation.
Scan protocol Slides were scanned with Affimetrix 428 Array Scanner using Software Jaguar 2.0. Images were analyzed Gene Pix Pro 6.0 (Molecular Devices Corporation). The median feature and local background intensities were extracted together with the estimates of their standard deviation.
Description No additional data.
Data processing Features were filtered out according to the following criteria: coefficient of variation (CV, ratio between standard deviation of the background and the median feature intensity) above 0.5 and foreground to background ratio above 1.5. Saturated features were removed. Log2 ratios were normalized using LOESS fit to spike in control RNAs and housekeeping controls. Filtration and normalization was done in Orange software. Normalized log ratios can be compared across samples.
 
Submission date Aug 19, 2008
Last update date Aug 22, 2008
Contact name Peter Juvan
Phone +386 1 543 7595
Organization name Faculty of Medicine, University of Ljubljana
Department Institute of Biochemistry
Lab Center for Functional Genomics and Bio-Chips
Street address Zaloska 4
City Ljubljana
ZIP/Postal code SI-1000
Country Slovenia
 
Platform ID GPL7138
Series (2)
GSE12489 Effect of phenobarbital on CAR and PXR regulated genes involved in drug metabolism and cholesterol homeostasis
GSE12529 Phenobarbital and TCPOBOP effects on CAR and PXR regulated genes involved in drug metabolism and cholesterol homeostasis

Data table header descriptions
ID_REF
VALUE Normalized log2 ratio (treated/control)

Data table
ID_REF VALUE
ST_Mm_082
ST_Mm_083
ST_Mm_087
ST_Mm_084 0.135
ST_Mm_085 0.500
ST_Mm_150 1.233
ST_Mm_088 0.502
ST_Mm_154 1.218
ST_Mm_155 0.809
ST_Mm_156 0.605
ST_Mm_157 0.917
ST_Mm_008 0.339
ST_Mm_009 0.305
ST_Mm_002 0.284
ST_Mm_003
ST_Mm_001 0.410
ST_Mm_006 -0.102
ST_Mm_007 0.596
ST_Mm_004
ST_Mm_005 0.299

Total number of rows: 151

Table truncated, full table size 2 Kbytes.




Supplementary file Size Download File type/resource
GSM313697.txt.gz 54.0 Kb (ftp)(http) TXT
Processed data included within Sample table

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