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Status |
Public on Oct 31, 2012 |
Title |
GFP-SAS siNon target |
Sample type |
RNA |
|
|
Source name |
GFP-SAS, siNT
|
Organism |
Homo sapiens |
Characteristics |
cell line: GFP-SAS cell type: squamous cell carcinoma cell line treatment: siNT
|
Treatment protocol |
GFP-SAS cells were treated with siNT, siAURKA-1 or -2 (10 nM), DMSO, or MLN8237 (100nM) for 24 h.
|
Growth protocol |
GFP-SAS cells were incubated in a humidified atmosphere of 95% air and 5% CO2 at 37℃.
|
Extracted molecule |
total RNA |
Extraction protocol |
ISOGEN extraction of total RNA was performed according to the manufacturer's instructions.
|
Label |
Biotin
|
Label protocol |
10 ng of total RNA was labeled using a GeneAtlasTM 3'IVT Express Kit Assay (Affymetrix) according to the manufacturer's instructions.
|
|
|
Hybridization protocol |
7.5 µg fragmented and labeled aRNA were hybridized for 16h at 45℃ on Human Genome U219 Array Strips. Array Strips were washed and stained in the GeneAtlasTM Fluidics Station.
|
Scan protocol |
Array Strips were scanned in the GeneAtlasTM imaging station.
|
Description |
Tongue
|
Data processing |
The robust multichip average (RMA) method was used for background correction and normalization using GeneSpring GX 12.1 software.
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|
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Submission date |
Oct 18, 2012 |
Last update date |
Oct 31, 2012 |
Contact name |
Hiroshi Tanaka |
E-mail(s) |
tanachu3@m.ehime-u.ac.jp
|
Organization name |
Ehime University
|
Department |
Oral and Maxillofacial Surgery
|
Street address |
454 Shitsukawa
|
City |
Toon |
State/province |
Ehime |
ZIP/Postal code |
791-0295 |
Country |
Japan |
|
|
Platform ID |
GPL13667 |
Series (1) |
GSE41697 |
Microarray analysis of GFP-SAS cells treated with siAURKA and MLN8237 |
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