|
Status |
Public on Mar 22, 2016 |
Title |
SKOV3_CFG_TGFbeta-1 |
Sample type |
RNA |
|
|
Source name |
human ovarian cancer cell line
|
Organism |
Homo sapiens |
Characteristics |
gender: female cell line: SKOV3
|
Treatment protocol |
After serum starvation for 24 h, the ovarian cancer cells were treated with 3 mg/ml CFG only or in combination with 10 ng/ml TGFβ1 for 24 h
|
Growth protocol |
maintained in DMEM supplemented with 10% fetal bovine serum at 37℃ in a humidified 5% CO2 atmosphere.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted from treated and non-treated cell lines using Trizol reagent (Invitrogen, Carlsbad, San Diego, USA) following the manufacturer’s protocol
|
Label |
biotin
|
Label protocol |
The amplified RNA was prepared with the GeneChip 3’IVT Express Kit (Affymetrix Inc., Santa Clara, CA, USA).
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|
|
Hybridization protocol |
After fragmentation, the amplified transcripts were hybridized to an Affymetrix 901838 GeneChip PrimeView Human Gene Expression Array (Affymetrix Inc.) for 16 h in a GeneChip Hybridization Oven 645
|
Scan protocol |
Arrays were washed and stained by a GeneChip Fluidics Station 450 and scanned by a GeneChip Scanner 3000
|
Data processing |
Raw data were imported into GeneSpring GX 11.0.1 and analyzed
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|
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Submission date |
Mar 21, 2016 |
Last update date |
Mar 22, 2016 |
Contact name |
Fangfang Tao |
E-mail(s) |
[email protected]
|
Organization name |
Zhejiang Chinese Medical University
|
Street address |
540 Binwen Road,binjiang district
|
City |
Hangzhou |
State/province |
Zhejiang |
ZIP/Postal code |
310053 |
Country |
China |
|
|
Platform ID |
GPL16043 |
Series (1) |
GSE79454 |
Microarray to identify the differentially expressed genes in CFG treated SKOV3 cells compared with control cells under TGFbeta condition |
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