|
Status |
Public on Dec 31, 2018 |
Title |
6_1_PD1 |
Sample type |
RNA |
|
|
Source name |
peripheral blood
|
Organism |
Homo sapiens |
Characteristics |
cell type: CD4+ T cell treatment protocol: 8 hrs CD3CD28 activation + PD1
|
Treatment protocol |
Immediately after isolation or after described treatment, cells were lysed in Trizol reagent.
|
Growth protocol |
Freshly isolated CD4+CD25low/intCD127+ T cells; CD4+ T cells were cultured as indicated. CD4+CD25+ Treg cells were expanded in cell culture.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with Trizol reagent, followed by clean-up and DNase I treatment with QIAGEN RNeasy mini kit in accordance with the prescribed protocol provided with the kit. Quality control was performed with NanoDrop ThermoScientific.
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays
|
|
|
Hybridization protocol |
Standard Illumina hybridization protocol
|
Scan protocol |
Standard Illumina scanning protocol
|
Description |
replicate 1
|
Data processing |
The data were normalised using quantile normalisation in R
|
|
|
Submission date |
Jun 25, 2009 |
Last update date |
Dec 31, 2018 |
Contact name |
Joachim Schultze |
E-mail(s) |
j.schultze@uni-bonn.de
|
Organization name |
LIMES (Life and Medical Sciences Center Genomics and Immunoregulation)
|
Department |
Genomics and Immunoregulation
|
Street address |
Carl-Troll-Strasse 31
|
City |
Bonn |
State/province |
NRW |
ZIP/Postal code |
53115 |
Country |
Germany |
|
|
Platform ID |
GPL2507 |
Series (2) |
GSE15390 |
FOXP3-mediated inhibition of the global gene regulator SATB1 is required for maintaining regulatory T cell commitment |
GSE16843 |
Comparison of the transcriptional profile of PD1-treated CD4+ T cells with a Treg cell phenotype and Tconv cells |
|