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Sample GSM228717 Query DataSets for GSM228717
Status Public on Sep 15, 2007
Title A549, 48 h, ethanol control
Sample type RNA
 
Source name A549, 48 h, ethanol control
Organism Homo sapiens
Characteristics A549, epithelial, lung carcinoma
Extracted molecule total RNA
Extraction protocol A549 cells were treated with ethanol control or resveratrol (25 mM) for 48 h. One replicate of control cells and three replicates of resveratrol treated cells were analyzed. At the 48 h time point TRIzol (1 ml) was added to each culture flask, incubated and insoluble material removed by centrifugation at 10,000 RPM for 10 min at 4°C. Chloroform (0.2 ml) was added to each sample which was shaken and incubated for phase separation. Samples were centrifuged at 10,000 RPM for 15 min at 4°C and the RNA (top aqueous phase) isolated. RNA was precipitated by mixing with isopropanol (0.8 ml) and centrifuging at 10,000 RPM for 10 min at 4°C. The RNA pellet was washed with 75% ethanol, dried and dissolved in Rnase-free water. Cleanup of the RNA was performed using an RNeasy spin column (Qiagen).
Label Biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol at the University of Chicago Functional Genomics Facility according to the Affymetrix GeneChip Expression Analysis Manual (Santa Clara, CA). Briefly, 10 g of total RNA was used to synthesize double-stranded cDNA using the Superscript Choice System (Life Technologies). First strand cDNA synthesis was primed with a T7-(dT24) oligonucleotide. From the phase-log gel-purified cDNA, biotin-labeled anti-sense cRNA was synthesized using BioArray High Yield RNA Transcript Labeling Kit (Enzo Diagnostics, Farmingdale, NY). After precipitation with 4M Lithium Chloride, 20 g of cRNA was fragmented in fragmentation buffer (40 mM Tris-Acetate, pH 8.1, 100 mM KOAc, and 30 mM MgOAc) for 35 min at 94°C
 
Hybridization protocol Hybridizations were performed at the Functional Genomics Facility, University of Chicago.Following fragmentation, 12 g of fragmented cRNA was hybridized to U133 Plus 2.0 Arrays for 16 h at 45°C and 60 rpm in an Affymetrix Hybridization Oven 640. The arrays were washed and stained with streptavidin phycoerythrin in Affymetrix Fluidics Station 400 using the Affymetrix GeneChip protocol.
Scan protocol GeneChips were scanned using the Affymetrix Agilent GeneArray Scanner.
Description A549, 48 h, ethanol control
Data processing MAS5.0
 
Submission date Sep 11, 2007
Last update date Aug 28, 2018
Contact name Lorna Whyte
Organization name IIT Research Institute
Department Division of Carcinogenesis and Chemoprevention
Street address 10 W 35th Street
City Chicago
State/province IL
ZIP/Postal code 60616
Country USA
 
Platform ID GPL570
Series (1)
GSE9008 Resveratrol action on A549 lung cancer cells
Relations
Reanalyzed by GSE64985
Reanalyzed by GSE119087

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 343.517 P 0.00687065
AFFX-BioB-M_at 315.147 P 0.000445901
AFFX-BioB-3_at 166.136 P 0.0200219
AFFX-BioC-5_at 464.456 P 0.000972149
AFFX-BioC-3_at 330.887 P 0.000146581
AFFX-BioDn-5_at 725.814 P 0.000340305
AFFX-BioDn-3_at 3287.03 P 0.00110197
AFFX-CreX-5_at 6953.77 P 6.02111e-05
AFFX-CreX-3_at 8622.96 P 4.42873e-05
AFFX-DapX-5_at 18.1779 A 0.300591
AFFX-DapX-M_at 46.7627 A 0.287743
AFFX-DapX-3_at 5.30485 A 0.891021
AFFX-LysX-5_at 31.4769 A 0.275146
AFFX-LysX-M_at 62.2747 A 0.41138
AFFX-LysX-3_at 2.97874 A 0.60308
AFFX-PheX-5_at 3.51097 A 0.876428
AFFX-PheX-M_at 2.77416 A 0.963431
AFFX-PheX-3_at 33.0307 A 0.588627
AFFX-ThrX-5_at 11.8227 A 0.749204
AFFX-ThrX-M_at 5.55375 A 0.737191

Total number of rows: 54675

Table truncated, full table size 1626 Kbytes.




Supplementary file Size Download File type/resource
GSM228717.CEL.gz 5.4 Mb (ftp)(http) CEL
GSM228717.CHP.gz 291.4 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file

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