|
Status |
Public on Feb 13, 2014 |
Title |
AML1 no IL-3 6h |
Sample type |
RNA |
|
|
Source name |
Primary AML MNCs
|
Organism |
Homo sapiens |
Characteristics |
cell type: Primary AML MNCs treatment: no IL-3 6h disease: Acute myeloid leukaemia cytogenetics: t(9;11), 11q23
|
Treatment protocol |
Mononuclear AML cells thawed overnight and cultured in IMDM with 10% FBS were treated +/- 15ng/mL hIL-3 for 6 or 16h.
|
Growth protocol |
Mononuclear AML cells were thawed and recovered overnight in IMDM with 20% FBS and DNase (50U/mL). Non-viable cells were subsequently removed using Lymphoprep (Axis-Shield PLC). AML cells were then cultured in IMDM with 10% FBS and stimulated with IL-3 as described below.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was purified using the miRNeasy protocol (Qiagen)
|
Label |
Biotin
|
Label protocol |
Total RNA was converted to biotinylated sense DNA as per the Affymetrix Genechip Whole Transcript (WT) Sense Target Labeling Assay Manual.
|
|
|
Hybridization protocol |
Genechips were hybridised overnight at 45 degrees C for 17 hours in an Affymetrix Hybridisation oven.
|
Scan protocol |
Genechips were scanned using the Affymetrix GSC3000 scanner.
|
Data processing |
Raw CEL files were normalised with RMA method using aroma.affymetrix.
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|
|
Submission date |
Oct 18, 2013 |
Last update date |
Feb 13, 2014 |
Contact name |
Chung H Kok |
E-mail(s) |
chung.kok@sahmri.com
|
Organization name |
South Australia Health and Medical Research Institute
|
Street address |
North Terrace
|
City |
Adelaide |
State/province |
South Australia |
ZIP/Postal code |
5000 |
Country |
Australia |
|
|
Platform ID |
GPL6244 |
Series (1) |
GSE51402 |
Gene expression patterns in response to IL-3 in human AML patient mononuclear cells |
|