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Sample GSM1279614 Query DataSets for GSM1279614
Status Public on Dec 16, 2013
Title sar1a [TPB2006082919Aaa]
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 13.82546947
1367453_at 12.30506943
1367454_at 10.65397726
1367455_at 12.66992089
1367456_at 12.78960644
1367457_at 11.17259427
1367458_at 10.00431094
1367459_at 13.447918
1367460_at 13.03327405
1367461_at 11.08687954
1367462_at 11.99689414
1367463_at 12.56845312
1367464_at 11.69330128
1367465_at 11.3481779
1367466_at 12.40128872
1367467_at 12.07780065
1367468_at 8.888936118
1367469_at 13.45590391
1367470_at 12.10045045
1367471_at 10.85770117

Total number of rows: 31099

Table truncated, full table size 698 Kbytes.




Supplementary file Size Download File type/resource
GSM1279614_TPB2006082919Aaa.CEL.gz 4.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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