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Status |
Public on Jun 01, 2018 |
Title |
Cultured cell line with HCV treated with brusatol rep1 |
Sample type |
RNA |
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Source name |
HPI-Brl60
|
Organism |
Homo sapiens |
Characteristics |
tissue: Hepatoma cell line
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Treatment protocol |
Bruratol was administered at the concentration of GI50 after precultuted cell.
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Growth protocol |
The cells were maintained in DMEM with 10% FBS for 1 dyay as precultue and for 2 days after the administration of brusatol prior to RNA extraction.
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA of the cultured cell was exracted by using RNaasy Mini Kit (QIAGEN) according to the pmanufacture's protocol.
|
Label |
Cy5
|
Label protocol |
cDNA and Amino Allyl aRNA was synthesis by Amino Allyl MessageAmp II aRNA Amplification Kit (Ambion#1753). CyeDye Coupling and fragmentation were performed as the protocol supplied by TORAY Industries, Inc..
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Hybridization protocol |
Hybridized for 16 h at 37 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 extracted
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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 |
May 15, 2017 |
Last update date |
Jun 01, 2018 |
Contact name |
Satoshi Kondo |
Organization name |
Toray Industries,Inc.
|
Department |
New Projects Development Division
|
Street address |
Tebiro 6-10-1
|
City |
Kamakura |
State/province |
Kanagawa |
ZIP/Postal code |
248-8555 |
Country |
Japan |
|
|
Platform ID |
GPL13915 |
Series (1) |
GSE98920 |
Dual effect of the Nrf2 inhibitor for inhibition of HCV and cell proliferation |
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