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Status |
Public on Jul 01, 2011 |
Title |
MS patient 3 |
Sample type |
RNA |
|
|
Source name |
peripheral blood mononuclear cells
|
Organism |
Homo sapiens |
Characteristics |
cell type: peripheral blood mononuclear disease state: multiple sclerosis
|
Treatment protocol |
Peripheral blood mononuclear cells were isolated from whole blood using BD Vacutainer® CPT™ Cell Preparation Tubes (Becton, Dickinson and Company, NJ, USA) according to the manufacturer's recommendations. Cells were homogenized in TRIzol® (Invitrogen, CA, US) and samples were stored in -80°C until RNA isolation.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with RNeasy Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 1-2 ug total RNA (GeneChip Expression Analysis Technical Manual, 2005-2006, Affymetrix).
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|
|
Hybridization protocol |
Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip® Human Genome U133 Plus 2.0 Array for 16 hours at 45°C and washed and stained in the Affymetrix Fluidics Station 450.
|
Scan protocol |
GeneChips were scanned using the Affymetrix GeneChip Scanner 3000.
|
Description |
Gene expression data from MS patients
|
Data processing |
The data were GC-RMA normalized and analyzed with GeneSpring 7.3 GX (Agilent Technologies, CA, US). After normalization and data filtering MS_11_REPL2 and MS_12_REPL2 were excluded from analysis.
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|
|
Submission date |
May 20, 2010 |
Last update date |
Jul 01, 2011 |
Contact name |
Anu Kemppinen |
E-mail(s) |
[email protected]
|
Organization name |
University of Cambridge
|
Street address |
Addenbrooke's Hospital, Hills Road
|
City |
Cambridge |
ZIP/Postal code |
CB2 0QQ |
Country |
United Kingdom |
|
|
Platform ID |
GPL570 |
Series (1) |
GSE21942 |
Expression data from peripheral blood mononuclear cells in multiple sclerosis patients and controls |
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