|
Status |
Public on May 12, 2007 |
Title |
DMSO treated MCF7 breast cancer cells [HG-U133A] Exp 2 |
Sample type |
RNA |
|
|
Source name |
MCF7 human breast cancer cells, DMSO-treated
|
Organism |
Homo sapiens |
Characteristics |
16 hr DMSO treatment
|
Extracted molecule |
total RNA |
Extraction protocol |
Qiagen RNeasy kit
|
Label |
biotin
|
Label protocol |
Enzo Biotin labeling
|
|
|
Hybridization protocol |
15ug of CRNA was fragmented, fragmented product was checked on gel(average size 100nt), Hybridization cocktail added and hybed on HG_U133A arrays. Washed with non-stringent wash buffer (A) and stained with SAPE solution.
|
Scan protocol |
HP Genechip Scanner (fixed pixel and wavelength)
|
Description |
MCF7 human breast cancer cells treated with DMSO and used as a control in a 2 platform, three replicate experiment
|
Data processing |
Probe array type- HG_U133 A. Parameters - defaults. Normalization - all probe sets. Scaling - all probe sets (Target signal - 2500)
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|
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Submission date |
May 08, 2007 |
Last update date |
May 11, 2007 |
Contact name |
Oliver Hankinson |
E-mail(s) |
[email protected]
|
Phone |
(310) 825-2936
|
Fax |
(310) 794-9272
|
Organization name |
UCLA
|
Department |
Pathology and Laboratory Medicine
|
Lab |
CHS-Hankinson
|
Street address |
PO Box 951732
|
City |
Los Angeles |
State/province |
CA |
ZIP/Postal code |
90095-1732 |
Country |
USA |
|
|
Platform ID |
GPL96 |
Series (1) |
GSE7765 |
Dioxin-induced gene expression changes in MCF-7 human breast cancer cells |
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