|
Status |
Public on Mar 01, 2016 |
Title |
SCOS#12 Dox OFF 72h |
Sample type |
RNA |
|
|
Source name |
osteosarcoma cell lines
|
Organism |
Mus musculus |
Characteristics |
cell line: SCOS#12 cell type: osteosarcoma cell lines treatment: none
|
Treatment protocol |
SCOS#2 and #12 Dox ON samples were treated with Dox (2µg/ml) containing medium for 72hours. SCOS#2 and #12 Dox OFF samples were mainteined with Dox-free medium for 72hours. RNA of sarcoma iPSCs was collected after removal of feeder cells (MEF).
|
Growth protocol |
DMEM+10%FBS+PS (SCOS#2 and #12) / Knockout DMEM+15%FBS+PS+L-glutamine+βME+LIF (Sarcoma iPSC)
|
Extracted molecule |
total RNA |
Extraction protocol |
RNeasy Plus Mini kit
|
Label |
Biotin
|
Label protocol |
Samples were enzymatically fragmented and biotinylated using the WT Terminal Labeling Kit (Affymetrix)
|
|
|
Hybridization protocol |
Samples were hybridized using Affymetrix hybridization kit materials • Heat cocktails at 99℃ for 5 minutes, then 45℃ for 5 minutes centrifuge at max speed for 1 minute (N.B. this deviates from Affy SOP). • Transfer 80μl of hyb solution to each array, then tape holes and parafilm. • Hybridize 17 hours at 45° at 60rpm• Fluidics washing is FS450_0007
|
Scan protocol |
Affymetrix Gene ChIP Scanner 3000 TG
|
Data processing |
Data were processed using Genespring software.
|
|
|
Submission date |
Sep 03, 2015 |
Last update date |
Mar 01, 2016 |
Contact name |
Yasuhiro Yamada |
E-mail(s) |
yyamada@m.u-tokyo.ac.jp
|
Organization name |
University of Tokyo
|
Department |
Department of Molecular Pathology
|
Street address |
7-3-1 Hongo, Bunkyo-ku
|
City |
Tokyo |
ZIP/Postal code |
113-0033 |
Country |
Japan |
|
|
Platform ID |
GPL6246 |
Series (2) |
GSE72704 |
EWS-FLI1-induced osteosarcoma model unveiled a crucial role of impaired osteogenic differentiation on osteosarcoma development [gene expression] |
GSE72898 |
EWS-FLI1-induced osteosarcoma model unveiled a crucial role of impaired osteogenic differentiation on osteosarcoma development |
|