|
Status |
Public on Apr 16, 2009 |
Title |
Human osteoblast sample 544 repl 2 |
Sample type |
RNA |
|
|
Source name |
Primary human osteoblasts
|
Organism |
Homo sapiens |
Characteristics |
tissue: Trabecular bone gender: female
|
Growth protocol |
The cells were grown in medium containing α-MEM supplemented with 2 mmol/l L-Glutamine, 100U/mL penicillin, 100mg/mL streptomycin and 10% fetal bovine serum at 37°C with 5% CO2. At 70-80% confluence, the cells were passaged and sub-cultured in 6-well plates (100,000 cells/well) for 12 days after which the cells were harvested and stored at -70°C until RNA extraction.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted from cell lysates resuspended in 600µl RLT lysis buffer using the RNeasy® Mini Kit. High RNA quality was confirmed for all samples using the Agilent 2100 BioAnalyzer and the concentrations were determined using Nanodrop ND-1000.
|
Label |
Biotin
|
Label protocol |
Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays
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|
|
Hybridization protocol |
Standard Illumina hybridization protocol
|
Scan protocol |
Standard Illumina scanning protocol
|
Description |
none
|
Data processing |
The data were normalized using variance-stabilizing transformation and robust spline normalization
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|
|
Submission date |
Apr 15, 2009 |
Last update date |
Apr 15, 2009 |
Contact name |
Elin Grundberg |
E-mail(s) |
[email protected]
|
Organization name |
McGill University and Genome Quebec Innovation Centre
|
Street address |
740 Dr Penfield Avenue
|
City |
Montreal |
ZIP/Postal code |
H3A1A4 |
Country |
Canada |
|
|
Platform ID |
GPL6104 |
Series (1) |
GSE15678 |
Population genomics in a disease targeted primary cell model |
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