|
Status |
Public on Jan 26, 2013 |
Title |
TOV21G - proliferating-rep3 |
Sample type |
RNA |
|
|
Source name |
TOV21G - proliferating
|
Organism |
Homo sapiens |
Characteristics |
cell type: Exponentially proliferating ovarian cancer cells cell line: TOV21G
|
Treatment protocol |
No treatment
|
Growth protocol |
Ovarian cancer cell lines were plated and harvested when 50-80% confluent. RNA was extracted and hybridized on Affymetrix microarrays. At least 3 biological repeats were performed for each cell line.
|
Extracted molecule |
total RNA |
Extraction protocol |
QIAgen Rneasy was used to extract RNA
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 1 ug total RNA
|
|
|
Hybridization protocol |
Hybridization was for 16hrs andaccording to the standard Affymetrix protocol
|
Scan protocol |
GeneChips were washed and stained in the Affymetrix GeneChip Fluidics Station 450 using standard Fluidics Protocol ((Fluidics protocol FS450_007)). GeneChips were scanned using the Affymetrix 7G Scanner
|
Data processing |
The data was gc-rma normalised using the R Bioconductor package affy.
|
|
|
Submission date |
Jan 25, 2013 |
Last update date |
Sep 01, 2016 |
Contact name |
Karen Elizabeth Sheppard |
E-mail(s) |
[email protected]
|
Phone |
61 3 9656 3758
|
Fax |
61 3 96563738
|
Organization name |
Perter MacCallum Cancer Centre
|
Department |
Research
|
Street address |
St Andrews Place
|
City |
Melbourne |
State/province |
Victoria |
ZIP/Postal code |
3008 |
Country |
Australia |
|
|
Platform ID |
GPL6244 |
Series (1) |
GSE43765 |
Expression data from exponentially proliferating ovarian cancer cell lines |
|
Relations |
Reanalyzed by |
GSE86357 |