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Status |
Public on Dec 16, 2013 |
Title |
sar1a [TPB2006082920Aaa] |
Sample type |
RNA |
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Source name |
McArdle RH7777 cell line overexpressing Sar1A
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Organism |
Rattus norvegicus |
Characteristics |
transgene status: overexpressing human SAR1A
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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.
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted with the RNeasy Plus Mini Kit (Qiagen) according to the manufacturer’s instructions.
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Label |
biotin
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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.
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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.
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Scan protocol |
Genechips were scanned with an Affymetrix Scanner 3000.
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Description |
Gene expression data from McArdle RH7777 rat hepatoma cell line overexpressing human SAR1A
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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.
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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 |
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Platform ID |
GPL1355 |
Series (1) |
GSE52969 |
Expression data from Sar1 isoform overexpressing rat hepatoma cell lines |
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