NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1347929 Query DataSets for GSM1347929
Status Public on Jul 24, 2014
Title Primary Mouse Hepatocytes exposed to 0.5 % v/v DMSO for 48h, biological rep 1
Sample type RNA
 
Source name primary mouse hepatocytes_0.5 % v/v DMSO for 48h
Organism Mus musculus
Characteristics strain background: C57Bl6
cell type: primary mouse hepatocytes
exposed to: 0.5 % v/v DMSO for 48h
Treatment protocol After the recovery period (40-42 hours), the medium was replaced with fresh medium containing either compound or solvent (0.5% DMSO)
Growth protocol Primary Mouse Hepatocytes were cultured in 6-well plates in a collagen-collagen sandwich and in the presence of serum-free culture medium supplemented with glucagon (7ng/mL), insulin (0.5 U/mL), 2% penicillin/streptomycin and hydrocortison (7.5 µg/mL). The cells were incubated at 37 C and 5% CO2.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated after 24 and 48 hours of incubation with CsA or DMSO in HepG2 total RNA was isolated from cells using miRNeasy mini Kit (Qiagen Westburg bv, Leusden, the Netherlands) according to the manufacturer’s instructions and followed by a DNAse I (Qiagen Inc.) treatment. RNA quantity was measured on a spectrophotometer and quality was determined on a BioAnalyzer (Agilent Technologies, Breda, the Netherlands). Only RNA samples which showed clear 18S and 28S peaks and with a RIN level higher than 8 were used.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 250ng total RNA using the 3’ IVT express kit
 
Hybridization protocol 12.5µg of cRNA were hybridized for 16 hr on 45°C on Affymetrix Mouse Genome 430 2.0 Array, using Affymetrix® GeneChip® Fluidics Station 450 and the GeneChip Hybridization, Wash and Stain Kit
Scan protocol Arrays were scanned using Affymetrix GeneArray scanner.
Description DMSO_48h_Exp1_33
Data processing Obtained data sets were re-annotated to the MBNI Custom CDF-files v15.1 (http://brainarray.mbni.med.umich.edu/Brainarray/Database/CustomCDF/genomic_curated_CDF.asp) (Dai et al., 2005) and RMA normalized (Irizarry et al., 2003) using the Arrayanalysis.org web service.
The 'complete_data.txt' (of 17,370 data rows) contains ~60 of control probes, which are not included in the sample data table.
 
Submission date Mar 13, 2014
Last update date Jul 24, 2014
Contact name Wim Van den Hof
E-mail(s) vandenhof.wim@gmail.com
Organization name Maastricht University
Department Toxicogenomics
Street address Universiteitssingel 50
City Maastricht
ZIP/Postal code P.O. Box 616, 6200 MD
Country Netherlands
 
Platform ID GPL15967
Series (2)
GSE55881 Expression Profiles of Primary Mouse Hepatocytes treated with Cyclosporin A and solvent control [RNA]
GSE55883 Expression Profiles of Primary Mouse Hepatocytes treated with Cyclosporin A and solvent control

Data table header descriptions
ID_REF
VALUE Log2 of RMA intensity from MBNI custom annotation

Data table
ID_REF VALUE
100008567_at 6.417623597
100009600_at 5.472057357
100012_at 3.181831478
100017_at 8.14479725
100019_at 7.744554856
100034251_at 6.127729363
100034739_at 3.652909721
100034748_at 4.170279903
100036520_at 3.86845534
100036521_at 9.381222075
100036523_at 4.694906064
100036768_at 3.905590879
100037258_at 9.385096049
100037262_at 5.398992882
100037278_at 7.10622429
100038347_at 4.95136065
100038358_at 3.819105794
100038371_at 3.632310423
100038392_at 5.100085781
100038398_at 7.832660938

Total number of rows: 17306

Table truncated, full table size 359 Kbytes.




Supplementary file Size Download File type/resource
GSM1347929_AK9.CEL.gz 3.6 Mb (ftp)(http) CEL
Raw data provided as supplementary file
Processed data included within Sample table
Processed data are available on Series record

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