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Status |
Public on Dec 01, 2010 |
Title |
ade2dsRNA-2a |
Sample type |
RNA |
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Source name |
S2 cells+ade2 dsRNA2
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Organism |
Drosophila melanogaster |
Characteristics |
cell type: S2 cells protocol: RNAi-mediated knockdown of ade2 (ade2 RNAi) RNAi name: ade2 dsRNA2
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Treatment protocol |
dsRNA treatment followed the protocol of Maiato et al (2003) Biol. Proced. Online 5:153-161.
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Growth protocol |
S2-6 cells were obtained from the Drosophila Genetics Resources Center and cultured in Schneider cell meda (Invitrogen) supplemented with 10% FBS (Invitrogen)
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Extracted molecule |
total RNA |
Extraction protocol |
Trizol (Invitrogen)
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Label |
Cy3
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Label protocol |
RNA was linearly amplified and labeled with Cy3, and labeled cRNA quantity and specific activity were assessed with the NanoDrop ND-1000 (Thermo Scienctific).
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Hybridization protocol |
1.65 ug of labeled cRNA was fragmented for 30 min and applied to Agilent microarrays 4x44K format (G2519F) and hybridized for 17 hrs at 65 C in the Agilent hybridization oven, and washed with Agilent wash buffers
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Scan protocol |
Agilent DNA Microarray Scanner at 5um resolution
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Description |
gene expression after 4 days ade2dsRNA-2a
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Data processing |
Agilent Feature extraction 9.1 software. Intensities per spot had their local background subtracted. A step of spatial detrending was done using negative control spots across the whole array and subtracting a surface fit from the data. Then data were loaded into GeneSpring 7.3 and all raw values below 5 were set to 5. The data were normalized to the median, so that intensities were divided by the median of all intensities.
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Submission date |
Sep 14, 2010 |
Last update date |
Sep 14, 2010 |
Contact name |
Denise Clark |
E-mail(s) |
[email protected]
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Phone |
506-452-6193
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Fax |
506-453-3583
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Organization name |
University of New Brunswick
|
Department |
Biology
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Street address |
10 Bailey Drive
|
City |
Fredericton |
State/province |
NB |
ZIP/Postal code |
E3B 5A3 |
Country |
Canada |
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Platform ID |
GPL7300 |
Series (1) |
GSE24123 |
Effects of purine de novo synthesis knockdown on gene expression in Drosophila melanogaster S2 tissue culture cells |
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