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Status |
Public on Dec 01, 2019 |
Title |
Control_2 |
Sample type |
RNA |
|
|
Source name |
Hepatoma cell
|
Organism |
Rattus norvegicus |
Characteristics |
cell line: FaO cell type: hepatocyte
|
Treatment protocol |
Fao cells were treated in the presence of 2% FCS and treated with a single dose of 0.1µM Thapsigargin and daily with 500 µM α-Lipoic acid. RNA was extracted after treatment with TG for 6 and 18 hrs and after treatment with α-Lipoic acid for 6, 18, 24, 30, 42, 48 and72 hrs. Three wells for each sample were pooled
|
Growth protocol |
Hepatoma cells FaO were grown in DMEM Plus Glutamax I (Invitrogen, Life Technologies) supplemented with Pen Strep and 10% heat-inactivated FCS (Life Technologies) in a humidified atmosphere of 5% CO2/95% air, at 37°C
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with Trizol reagent. Quality control was performed with Agilent Bioanalyser.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays
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|
|
Hybridization protocol |
Standard Illumina hybridization protocol
|
Scan protocol |
Standard Illumina scanning protocol
|
Description |
Hepatoma cell FaO
|
Data processing |
The data were normalised using quantile normalisation with Illumina BeadStudio 3.0.19.0 software (Illumina Inc) and BRB Array Tools (Version 4.2.0)
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|
|
Submission date |
Jul 07, 2014 |
Last update date |
Dec 01, 2019 |
Contact name |
Gabriella Simbula |
E-mail(s) |
gsimbula@unica.it
|
Organization name |
THE UNIVERSITY OF CAGLIARI
|
Street address |
Porcel 4
|
City |
Cagliari |
State/province |
CA |
ZIP/Postal code |
09124 |
Country |
Italy |
|
|
Platform ID |
GPL6101 |
Series (1) |
GSE59164 |
Lipoic acid induced endoplasmic reticulum stress-mediated apoptosis in rat hepatoma cells:identification of new ER stress aggravator (ERSA) |
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