NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1279615 Query DataSets for GSM1279615
Status Public on Dec 16, 2013
Title sar1a [TPB2006082920Aaa]
Sample type RNA
 
Source name McArdle RH7777 cell line overexpressing Sar1A
Organism Rattus norvegicus
Characteristics transgene status: overexpressing human SAR1A
Growth protocol Cells were cultured in complete DMEM containing Blasticidin (10μg/ml; Sigma) and Zeocin (250μg/ml; Invitrogen). Twenty four hours prior to harvesting, 1μg/ml of tetracycline was added to the culture media.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with the RNeasy Plus Mini Kit (Qiagen) according to the manufacturer’s instructions.
Label biotin
Label protocol cDNA was synthesized from total RNA using the One-Cycle Eukaryotic Target Labeling Assay Kit (Invitrogen) (Affymetrix https://www.affymetrix.com/support/downloads/manuals/expression_s21_manual.pdf). Double-stranded cDNA was purified with the kit GeneChip® Sample Cleanup Module (Affymetrix). Biotinlabelled cRNA was prepared using the BioArray High Yield RNA Transcript Labelling Kit (Enzo) and purified with the IVT cRNA GeneChip® Sample Cleanup Module.
 
Hybridization protocol Following fragmentation, 15μg biotinylated cRNA was hybridized to GeneChip Rat Genome 230 2.0 arrays (Affymetrix) for 16 hr at 45°C in an Affymetrix Hybridization Oven 640. GeneChips were washed and stained in an Affymetrix Fluidics 450 Station according to standard Affymetrix protocols.
Scan protocol Genechips were scanned with an Affymetrix Scanner 3000.
Description Gene expression data from McArdle RH7777 rat hepatoma cell line overexpressing human SAR1A
Data processing Data analyses were performed through the Comprehensive R-based Microarray Analysis web service (CARMAweb: https:// CARMAweb.genome.tugraz.at /CARMA/). Raw intensity values were normalized using the Loess normalization, Affymetrix MAS 5 and summarization algorithms. Differences in probe-set values were determined on the normalized data using the Significance Analysis of Microarray (SAM) algorithm at specified False Discovery Rates. Cut-off values for significance determined by a tuning parameter, the delta value. The number of delta values was set at 50 and a Benjamini & Hochberg multiple testing correction was applied.
 
Submission date Dec 04, 2013
Last update date Dec 16, 2013
Contact name Carol Shoulders
Organization name QMUL
Department Centre for Endocrinology
Street address Charterhouse Square
City London
ZIP/Postal code EC1M 6BQ
Country United Kingdom
 
Platform ID GPL1355
Series (1)
GSE52969 Expression data from Sar1 isoform overexpressing rat hepatoma cell lines

Data table header descriptions
ID_REF
VALUE Normalized MAS5.0 signal intensity

Data table
ID_REF VALUE
1367452_at 14.02848653
1367453_at 12.28022053
1367454_at 10.72022166
1367455_at 12.70401586
1367456_at 12.88749283
1367457_at 11.29388066
1367458_at 10.03877928
1367459_at 13.51765052
1367460_at 13.08412236
1367461_at 11.10799215
1367462_at 11.94996971
1367463_at 12.58172641
1367464_at 11.73679261
1367465_at 11.39804223
1367466_at 12.39913278
1367467_at 12.06632318
1367468_at 8.818117429
1367469_at 13.58883973
1367470_at 11.99846425
1367471_at 10.89788125

Total number of rows: 31099

Table truncated, full table size 698 Kbytes.




Supplementary file Size Download File type/resource
GSM1279615_TPB2006082920Aaa.CEL.gz 4.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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