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Status |
Public on Jul 14, 2014 |
Title |
Superficial temporal artery, sample 3 |
Sample type |
RNA |
|
|
Source name |
Superficial temporal artery, sample 3
|
Organism |
Homo sapiens |
Characteristics |
tissue: Superficial temporal artery status: Superficial temporal artery Sex: Female age: 34
|
Treatment protocol |
All the specimens were snap-frozen in liquid nitrogen, and stored at -80 °C.
|
Growth protocol |
In case of ruptured intracranial aneurysms, all resections were done within 24 hours after initial subarachnoid hemorrhage.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted with the TRIzol reagent (Invitrogen, Carlsbad, CA, USA).
|
Label |
Cy3
|
Label protocol |
500 ng of total RNA was amplified and labeled with the Agilent Quick Amp Labeling Kit according to the manufacturers instructions.
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|
|
Hybridization protocol |
1.65 ug of cyanine 3-CTP (Cy3)-labeled cRNA sample was used for 17-hour hybridization at 65 C.
|
Scan protocol |
The Agilent DNA microarray scanner (model G2505A) was used. Signal intensity was quantified from the scanned image by using Feature Extraction Software version 9.1 (Agilent technologies)
|
Description |
Gene expression in superficial temporal artery
|
Data processing |
The signal intensities were corrected for the background intensities with the normexp method, followed by the quantile normalization across arrays with the limma software.
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|
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Submission date |
Jan 14, 2014 |
Last update date |
Jul 14, 2014 |
Contact name |
Hirofumi Nakaoka |
E-mail(s) |
[email protected]
|
Phone |
81-055-981-6795
|
Organization name |
National Institute of Genetics
|
Department |
Department of Human Genetics
|
Street address |
Yata 1111
|
City |
Mishima |
State/province |
Shizuoka |
ZIP/Postal code |
411-8540 |
Country |
Japan |
|
|
Platform ID |
GPL4133 |
Series (1) |
GSE54083 |
Gene expression profiling of intracranial aneurysms |
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