|
Status |
Public on Dec 21, 2015 |
Title |
SG-3 |
Sample type |
RNA |
|
|
Source name |
Salivary gland
|
Organism |
Homo sapiens |
Characteristics |
tissue: salivary gland
|
Extracted molecule |
total RNA |
Extraction protocol |
After fresh tissues were homogenized by TissueLyser, total RNA was extracted by ISOGEN.
|
Label |
digoxigenin
|
Label protocol |
Digoxigenin-UTP-labelled cRNA was generated and amplified from 1 mg of total RNA using Applied Biosystems Chemiluminescent RT-IVT Labelling Kit.
|
|
|
Hybridization protocol |
Ten mg of labelled cRNA was hybridized to each pre-hybridized microarray at 55℃ for 16 hours.
|
Scan protocol |
After Chemiluminescence detection using Applied Biosystems Chemiluminescence Detection Kit, images were collected by the AB1700 Chemiluminescent Microarray Analyzer.
|
Data processing |
The quantile method was used for background correction and normalization.
|
|
|
Submission date |
Jul 07, 2015 |
Last update date |
Dec 21, 2015 |
Contact name |
Koh-ichi Nakashiro |
E-mail(s) |
[email protected]
|
Phone |
+81899605393
|
Organization name |
Ehime University Graduate School of Medicine
|
Department |
Oral and Maxillofacial Surgery
|
Street address |
454 Shitsukawa
|
City |
Toon |
State/province |
Ehime |
ZIP/Postal code |
791-0295 |
Country |
Japan |
|
|
Platform ID |
GPL2986 |
Series (1) |
GSE70604 |
Gene expression profiles in lymph nodes with metastasis of oral squamous cell carcinoma (OSCC) |
|