|
Status |
Public on Jan 01, 2014 |
Title |
H44_1 |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
Hypopharyngeal squamous cell carcinoma No. 44
|
Organism |
Homo sapiens |
Characteristics |
tissue: Non tumor tissue age: 64 gender: Female t: 4a n: 1 m: 0 Stage: IVA differentiation: poor
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA extracted using Trizol following manufacturer's instructions
|
Label |
Hy3
|
Label protocol |
We used miRCURY LNA microRNA Array Hi-Power Labeling kit.
|
|
|
Channel 2 |
Source name |
H44 pooled sample
|
Organism |
Homo sapiens |
Characteristics |
pooled sample composition: blends equal amounts of each samples
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA extracted using Trizol following manufacturer's instructions
|
Label |
Hy5
|
Label protocol |
We used miRCURY LNA microRNA Array Hi-Power Labeling kit.
|
|
|
|
Hybridization protocol |
Denature the solution at 95 ℃ for 5 min. Centrifuge at 12,000 g at 4 ℃ for 2 min. Add 30 μL of 20 x salt Buffer to ditch of “Hybridization Chamber”. Slide is capped by “MASTUNAMI Gap Cover Glass (CG00044 or 24*60 25PCS)”. Fill the gap with 45 μL of the solution. Incubate in 56 ℃ water bath for 16-20 hr.
|
Scan protocol |
Scanner; G2505C (Agilent), Software; Agilent Scan Control (Agilent), Green and Red PMT: 100 %, Scan resolution: 10 um
|
Description |
CB-RNA76-10
|
Data processing |
Quantification; Feature Extraction 10.7.3.1 (Agilent). Normalization; First, calculate the average ratio (Hy3/Hy5) of replicated spots on each array. Next, calculate the ratio of average ratio (Tumor/Non tumor).
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|
|
Submission date |
Sep 24, 2013 |
Last update date |
Jan 01, 2014 |
Contact name |
Naohiko Seki |
Organization name |
Chiba University
|
Street address |
Inohana1-8-1, Chuo-ku
|
City |
Chiba city |
State/province |
Chiba |
ZIP/Postal code |
260-8670 |
Country |
Japan |
|
|
Platform ID |
GPL17728 |
Series (1) |
GSE51129 |
microRNA expression profile of hypopharyngeal squamous cell carcinoma |
|