|
Status |
Public on Jan 23, 2008 |
Title |
U937 cells treated with ultrasound (control-1) |
Sample type |
RNA |
|
|
Source name |
Human lymphoma U937 cells, untreated (control-1)
|
Organism |
Homo sapiens |
Characteristics |
Human lymphoma U937 cells
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted from the cells using an RNeasy Total RNA Extraction Kit (Qiagen K.K., Tokyo, Japan). Then, RNA samples were treated with RNase-free DNase.
|
Label |
biotin
|
Label protocol |
5 μg of total RNA was used to synthesize double-strand cDNA with a GeneChip® Expression 3’-Amplification Reagents One-Cycle cDNA Synthesis Kit (Affymetrix). Biotin-labeled cRNA was then synthesized from the cDNA using GeneChip® Expression 3’-Amplification Reagents for IVT Labeling (Affymetrix).
|
|
|
Hybridization protocol |
After fragmentation, the biotinylated cRNA was hybridized to arrays at 45°C for 16 h.
|
Scan protocol |
The arrays were washed, stained with streptavidin-phycoerythrin and scanned with a probe array scanner (Affymetrix).
|
Description |
Human lymphoma U937 cells were cultured at 37°C (non-treatment; control).
|
Data processing |
GeneChip Analysis Suite
|
|
|
Submission date |
Jan 18, 2008 |
Last update date |
Jan 22, 2008 |
Contact name |
Yoshiaki Tabuchi |
E-mail(s) |
[email protected]
|
Organization name |
University of Toyama
|
Department |
Life Science Research Center
|
Lab |
Division of Molecular Genetics Research
|
Street address |
2630 Sugitani
|
City |
Toyama |
State/province |
Toyama |
ZIP/Postal code |
930-0194 |
Country |
Japan |
|
|
Platform ID |
GPL96 |
Series (1) |
GSE10212 |
Identification of genes responsive to ultrasound in human leukemia U937 cells |
|