|
Status |
Public on May 20, 2006 |
Title |
KINECells_Chemokinetic |
Sample type |
RNA |
|
|
Source name |
H460_Selected_For_Chemokinesis
|
Organism |
Homo sapiens |
Characteristics |
H460 Lung Cancer Cells Selected for highly chemokinetic trait.
|
Biomaterial provider |
ATCC
|
Treatment protocol |
Cells were selected for behaviour under chemokinetic conditions (no gradient of chemoattractant [1.5%FBS]) using Boyden chambers.
|
Growth protocol |
Cells grown were in complete medium (DMEM + 5% FBS). No antibiotics were used for the experiment. Cells were cultured for 24 h prior to harvesting for RNA extraction.
|
Extracted molecule |
total RNA |
Extraction protocol |
Standard RNA extraction procedure using RNAeasy Mini kit (Qiagen).
|
Label |
Biotin
|
Label protocol |
cRNA was labeled with biotin using the Affymetrix Enzo Kit according to the manufacturer's protocol.
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|
|
Hybridization protocol |
Hybridization, washing and staining were performed in a Fluidics Station according to standard procedures. Briefly, 15 micrograms of biotinylated cRNA were hybridized to a U133A chip for 16 h, and labeld with anti-streptavidin biotinylated antibody with intermittent washing steps.
|
Scan protocol |
Affymetrix® GeneChip® Scanner3000 was used to scan the chip with preset pixel resolution and wavelength values.
|
Description |
N/A
|
Data processing |
Affymetrix MAS 5.0 Scaling Protocol. Original signal values are scaled to a mean of 1000.
|
|
|
Submission date |
May 18, 2006 |
Last update date |
May 19, 2006 |
Contact name |
Lilian Soon |
E-mail(s) |
[email protected]
|
Phone |
293515322
|
Fax |
2 9351 7682
|
Organization name |
The University of Sydney
|
Department |
Australian Key Centre for Microscopy and Microanalysis, EMU
|
Lab |
Cancer Cell Imaging
|
Street address |
LG14, Madsen Building, F09
|
City |
Sydney |
State/province |
NSW |
ZIP/Postal code |
2006 |
Country |
Australia |
|
|
Platform ID |
GPL96 |
Series (1) |
GSE4869 |
Chemokinetic versus Chemotactic Cancer Cells |
|