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Status |
Public on Dec 31, 2012 |
Title |
0.1% BSA-treated SMCs rep2 |
Sample type |
RNA |
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|
Source name |
Rat aortic smooth muscle cells treated with vehicle (.1% BSA)
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Organism |
Rattus norvegicus |
Characteristics |
genotype: Sprague-Dawley cell type: aortic smooth muscle cell agent: BSA
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Treatment protocol |
Cells treated with either vehicle (.1% BSA) or IL-1b (2.5 ng/mL) for 24 hours.
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Growth protocol |
Smooth muscle cells were grown in 10% serum-containing media for 5 days, then switched to serum-free media for 3 days prior to treatment for 24 hours.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using Trizol reagent according to the manufacturer's instructions.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
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Hybridization protocol |
10 ug of cRNA was hybridized for 16 hours on Affymetrix rat 230 2.0 GeneChips and stained using Affymetrix Fluidics Station 450 according to Affymetrix protocols.
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Scan protocol |
GeneChips were scanned using the Affymetrix Scanner 3000.
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Description |
Gene expression data from vehicle-treated rat aortic smooth muscle cells
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Data processing |
The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) and between-group fold changes were calculated using Affymetrix Data Mining Tool 3.0. Local pooled error testing was performed by the University of Virginia Gene Expression Open Source System (GEOSS) software.
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Submission date |
Apr 20, 2010 |
Last update date |
Dec 31, 2012 |
Contact name |
Gary Owens |
Organization name |
University of Virginia
|
Department |
Molecular Physiology and Biological Physics
|
Lab |
Gary Owens' Laboratory
|
Street address |
415 Lane Road
|
City |
Charlottesville |
State/province |
VA |
ZIP/Postal code |
22908 |
Country |
USA |
|
|
Platform ID |
GPL1355 |
Series (1) |
GSE21403 |
Effect of IL-1b treatment on cultured rat aortic smooth muscle cells |
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