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Status |
Public on Oct 18, 2012 |
Title |
Cdk9 dsRNA and VSV infection at T4 hours_biological rep2 |
Sample type |
RNA |
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Source name |
Drosophila cells treated with Cdk9 dsRNA and infected with VSV at T4 hours, biological rep2
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Organism |
Drosophila melanogaster |
Characteristics |
cell line: DL1 treatment: Cdk9 dsRNA infection: VSV
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Treatment protocol |
Cells were infected with VSV (MOI 10) for 4 hours.
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Growth protocol |
3 million Drosophila cells (DL1) were treated with 4 ug Bgal or Cdk9 dsRNA and incubated for 3 days as described in (Cherry et al. 2005), then infected with VSV
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Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA was performed according to the manufacturer's instructions.
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Label |
Biotin
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Label protocol |
Upon fragmentation, 100ng RNA were amplified with the Ovation RNA Amplification System v2 (NuGen), Encore Biotin Module (NuGen) was used for labeling.
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Hybridization protocol |
The Standard Affymetrix hyb/wash/satining protocolwas used (Protocol FS450 002).
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Scan protocol |
For Scanning and Image, the GeneChip® Scanner 300) and Affymetrix® GeneChip® Command Console® Software (AGCC) were used.
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Description |
Gene expression data for transcript levels in Drosophila cells upon VSV infection and Cdk9 dsRNA treatment for 4 hours
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Data processing |
Arrays were analyzed using the Affy (Irizarry et al., 2003) and limma packages (Smyth, 2004) for R and Microsoft Excel. We calculated fold changes relative to uninfected controls and considered significant genes with at least a 2.8 fold change.
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Submission date |
Oct 01, 2012 |
Last update date |
Oct 18, 2012 |
Contact name |
Sara Cherry |
E-mail(s) |
[email protected]
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Organization name |
University of Pennsylvania
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Street address |
304K Lynch Labs
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City |
Philadelphia |
ZIP/Postal code |
19104 |
Country |
USA |
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Platform ID |
GPL1322 |
Series (1) |
GSE41242 |
Global analysis of Cdk9-dependence for VSV-induced genes in Drosophila cells |
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