|
Status |
Public on Aug 26, 2013 |
Title |
Th1Th17, patient 661 |
Sample type |
RNA |
|
|
Source name |
Peripheral blood mononuclear cells (PBMC)
|
Organism |
Homo sapiens |
Characteristics |
donor: 661 cell type: CD4+ Th cells cell subset: Th1Th17 cells
|
Treatment protocol |
Sorted Th1Th17 and Th1 subsets were stimulated with immobilized CD3 and soluble CD28 Abs (1 µg/ml) for 3 days
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated using the RNeasy kit (Qiagen, Valencia, CA) according to the manufacturer’s protocol and quantified by Pearl nanophotometer (Implen, Munich, Germany) (typically, 106 cells yielded 3-5 µg RNA).
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 6 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
|
|
|
Hybridization protocol |
Briefly, the quality of total RNA was first tested using an Agilent 2100 Bioanalyzer chip. Then, high quality RNA was reverse transcribed and hybridized on the GeneChip® Human Genome U133 Plus 2.0 Array (Affymetrix).
|
Scan protocol |
GeneChip scan was carried out at McGill University & Genome Quebec Innovation Centre according to the Affymetrix recommendation (Affymetrix Expression Manual Section 3 701029 rev. 4).
|
Description |
Gene expression data from circulating Th1Th17 cells
|
Data processing |
Gene expression data was analyzed using Bioconductor limma package. The R software package was used to preprocess and normalize the probes intensities using RMA.
|
|
|
Submission date |
Aug 25, 2013 |
Last update date |
Sep 01, 2016 |
Contact name |
Jean-Philippe Goulet |
E-mail(s) |
jp.goulet@umontreal.ca
|
Organization name |
Université de Montréal
|
Street address |
C.P. 6128, succursale Centre-ville
|
City |
Montréal |
State/province |
Québec |
ZIP/Postal code |
H3X 3J7 |
Country |
Canada |
|
|
Platform ID |
GPL570 |
Series (1) |
GSE50175 |
Expression data from human Th1 and Th1Th17 cells |
|
Relations |
Reanalyzed by |
GSE86362 |