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Status |
Public on Jul 15, 2014 |
Title |
Control siRNA at T48, biological rep 1 |
Sample type |
RNA |
|
|
Source name |
AsPC-1 transfected with 20nM control siRNA at 48 hours
|
Organism |
Homo sapiens |
Characteristics |
cell line: AsPC-1 treatment: transfected with 20nM Ctrl siRNA, 48h
|
Treatment protocol |
See growth protocol
|
Growth protocol |
AsPC-1 cells were grown to 70% confluency in standard growth conditions (RPMI + 10% FCS) and maintained in these conditions for the period (6 or 24 hours) with either 10uM ICG-001 or vehicle (DMSO, V/V). Separately, AsPC1 cells were also transfected with 20 nM control or CTNNB1 siRNA using lipofectamine 2000 with RNA extracted at 48 hours.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted using Qiagen Rneasy mini kit per manufacturer's instructions.
|
Label |
Biotin
|
Label protocol |
Affymetrix standard procol
|
|
|
Hybridization protocol |
Affymetrix standard procol
|
Scan protocol |
Affymetrix standard procol
|
Description |
Gene expression data for AsPC1 cells transfected with control siRNA for 48 hours
|
Data processing |
Data analysis was performed in the dChip Analysis software package(31) using invariant set normalization and signal intensities summarized using the MBEI (model-based expression index) algorithm with mismatch probe option for background subtraction. Initial gene filtering criteria was set at >10% present call and variance across samples of 0.4<standard deviation/mean<1000.
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|
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Submission date |
May 16, 2014 |
Last update date |
Jul 15, 2014 |
Contact name |
David Dawson |
Organization name |
UCLA
|
Department |
Pathology and Laboratory Medicine
|
Street address |
10833 LeConte Avenue
|
City |
Los Angeles |
State/province |
CA |
ZIP/Postal code |
90095-1732 |
Country |
USA |
|
|
Platform ID |
GPL570 |
Series (1) |
GSE57728 |
Expression data from AsPC1 cells treated with ICG-001 |
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