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Status |
Public on Dec 22, 2013 |
Title |
MOCK9 |
Sample type |
RNA |
|
|
Source name |
MOCK9
|
Organism |
Mus musculus |
Characteristics |
cell type: Mouse RAW cells
|
Treatment protocol |
RAW264.7 cells were infected with MNV-1 at a multiplicity of infection of 1, or mock infected, for 9 and 18 hours
|
Growth protocol |
RAW264.7 cells were grown at 37˚C + 5% CO2 in GIBCO DMEM with 4.5 g/L glucose + 2.5 mM HEPES + 5% fetal calf serum, in 6-well plates. Once cells were 70% confluent, infection was performed
|
Extracted molecule |
total RNA |
Extraction protocol |
Qiagen RNeasy mini kit
|
Label |
Biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
|
|
|
Hybridization protocol |
Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Mouse 430_2 array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
|
Scan protocol |
GeneChips were scanned using an Affymtrix scanner
|
Description |
Mouse RAW cells mock transfected after 18 h
|
Data processing |
The data were analyzed with GenePattern, using RMA and quantile normalisation using the ExpressionFileCreator in Genepattern (Reich et al., 2006), preprocessed using PreprocessDataset, comparison was done using ComparativeMarkerSelection.
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|
|
Submission date |
Aug 22, 2013 |
Last update date |
Dec 22, 2013 |
Contact name |
Christopher Michael Brown |
E-mail(s) |
[email protected]
|
Organization name |
University of Otago
|
Department |
Biochemistry
|
Street address |
710 Cumberland St
|
City |
Dunedin |
ZIP/Postal code |
9000 |
Country |
New Zealand |
|
|
Platform ID |
GPL1261 |
Series (1) |
GSE50093 |
Characterization of the chemokine response of RAW264.7 cells to infection by murine norovirus |
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