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Status |
Public on Oct 17, 2019 |
Title |
Panc-1 control3 |
Sample type |
RNA |
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|
Source name |
Panc-1 control
|
Organism |
Homo sapiens |
Characteristics |
disease state: pancreatic ductal adenocarcinoma cell line: Panc-1 agent: control
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Treatment protocol |
Panc-1 cells were treated with 0 or 10 ng/ml of TGF-β for 72 hours.
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Growth protocol |
Panc-1 cells were obtained and cultured as recommended by the supplier.
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Extracted molecule |
total RNA |
Extraction protocol |
RNA samples were extracted from cells using miRNeasy mini kit (Qiagen).
|
Label |
Cy5
|
Label protocol |
Extracted total RNA was labeled with Cy5 using the 3D-Gene miRNA labeling kit (Toray, Kamakura, Japan)
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Hybridization protocol |
Hybridized for 16 h at 32 C with rotary shake (250 rpm). Hybridization buffer and washing protocol was followed by the protocol supplied by TORAY Industries, Inc..
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Scan protocol |
3D-Gene Scanner ((Toray Industries Inc., Tokyo, Japan) was used for scanning. Images were quantified using Extraction(Toray Industries Inc., Tokyo, Japan).
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Description |
Total RNA was isolated from Panc-1 cells and analyzed miRNA expression by microarray.
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Data processing |
The raw data of each spot was normalized by substitution with a mean intensity of the background signal determined by all blank spots’ signal intensities of 95% confidence intervals.
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Submission date |
Oct 17, 2018 |
Last update date |
Oct 19, 2019 |
Contact name |
Satoshi Kondo |
Organization name |
Toray Industries,Inc.
|
Street address |
10-1 tebiro 6-chome
|
City |
Kamakura |
State/province |
Kanagawa |
ZIP/Postal code |
248-8555 |
Country |
Japan |
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|
Platform ID |
GPL21263 |
Series (1) |
GSE121369 |
MiRNA expression profiling in pancreatic ductal adenocarcinoma (PDAC) cells treated with TGF-b |
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