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Sample GSM1035808 Query DataSets for GSM1035808
Status Public on Nov 13, 2012
Title SA-treated, biological rep4
Sample type RNA
Source name 3T3-L1 preadipocytes_SA-treated
Organism Mus musculus
Characteristics cell type: differentiated 3T3-L1 preadipocytes
treated with: 250 μM Stearic Acid for 48 hrs
sample group: SFA
Treatment protocol Stocks (25mM) of freshly prepared palmitic acid (PA, 16:0), palmitoleic acid (PMA, 16:1n7), stearic acid (SA, 18:0), and oleic acid (OA, 18:1n9) were dissolved in 100% ethanol (Sigma Aldrich, MO, USA). FA stock solutions were subsequently diluted 1:100 in serum-free maintenance media containing 2% (wt/vol) BSA for a final concentration of 250 µM. Differentiated preadipocytes were treated for 48 hrs with the various FA solutions starting on day 8. The control treatment consisted of cells treated with 2% (wt/vol) BSA and a 1:100 dilution of 100% EtOH for 48 hrs.
Growth protocol 3T3-L1 preadipocytes were seeded at a density of 6.0x10^4 cells per well in six-well plates. Cells were cultured at 37°C in 5% CO2 in basic media consisting of DMEM supplemented with 5% heat-inactivated FBS and 1% penicillin-streptomycin. Differentiation was induced at 2 days post confluence (i.e. day 0) by adding a standard differentiation cocktail consisting of Dex (1 µM), IMBX (0.5 mM), and insulin (5 µg/ml) to basic media. After 2 days the differentiation media was replaced with maintenance media, which consisted of basic media supplemented with only insulin (5 µg/ml). Maintenance media was changed every 2 days for the reminder of the experiment. On day 7 FBS was removed from the media and the duration of the experiment was conducted in serum-free conditions.
Extracted molecule total RNA
Extraction protocol After the treatment period, total RNA was extracted from differentiated preadipocytes using the Qiagen RNeasy Mini Kit (Qiagen, Mississauga, Ontario, Canada) according to the manufacturer’s protocol. Extracted RNA was quantified using a Nanodrop (Fisher Scientific, Waltham, Massachusetts), and stored at -80oC for future analyses. RNA quality was verified using the Agilent 2100 BioAnalyzer (Agilent Technologies Inc., Santa Clara, CA, USA), and only samples with an RNA integrity number (RIN) greater than 9.0 were used for microarray analyses.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 100 ng total RNA according to the manufacturer's instructions.
Hybridization protocol For each sample, 100 ng of total RNA was prepared for hybridization to Affymetrix Mouse Gene 1.1 ST array strips, according to the manufacturer’s instructions. Strips were then washed and stained on the Affymetrix GeneAtlas platform.
Scan protocol Strips were scanned on the Affymetrix GeneAtlas platform.
Description sa4
Data processing The data was imported into R (version 2.15.0)/Bioconductor (Biobase version 2.16.0) and normalized using the robust multichip average (RMA) implementation in the Affy package (version 1.34.0). Normalized data consists of transcript cluster IDs as identifiers.
Submission date Nov 12, 2012
Last update date Nov 13, 2012
Contact name David M Mutch
Phone +1-519-824-4120
Organization name University of Guelph
Department Human Health & Nutritional Sciences
Lab ANNU 308
Street address 50 Stone Road East
City Guelph
State/province Ontario
ZIP/Postal code N1G 2W1
Country Canada
Platform ID GPL11533
Series (1)
GSE42220 Gene expression data from differentiated 3T3-L1 preadipocytes treated with Palmitic Acid, Stearic Acid, Palmitoleic Acid, or Oleic Acid

Data table header descriptions
VALUE robust multichip average (RMA) signal

Data table
10338001 10.19142507
10338002 6.090402148
10338003 8.726359241
10338004 8.280283138
10338005 2.415531616
10338006 2.732705876
10338007 3.109043691
10338008 3.895621959
10338009 7.322779544
10338010 2.415873857
10338011 5.562478069
10338012 2.543359054
10338013 2.251932448
10338014 2.318420278
10338015 2.235952502
10338016 6.844265421
10338017 11.28724592
10338018 6.43595092
10338019 5.146081478
10338020 7.4058646

Total number of rows: 35556

Table truncated, full table size 725 Kbytes.

Supplementary file Size Download File type/resource 4.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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