|
Status |
Public on Jun 19, 2009 |
Title |
M1 MR+ |
Sample type |
RNA |
|
|
Source name |
bone marrow derived DC
|
Organism |
Mus musculus |
Characteristics |
cell type: dendritic cells (DCs) mannose receptor: positive
|
Treatment protocol |
Immediately after FACS sort, bone marrow derived DC were lysed in Trizol reagent
|
Growth protocol |
Freshly isolated bone marrow derived cells were differentiated for 1 week with GM-CSF into bone marrow derived DCs. Afterwards, cells were incubated with Alexa647-labeled OVA to distinguish mannose receptor positive from mannose receptor negative cells by FACS analysis.
|
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 2
|
Data processing |
The data were normalised using quantile normalisation in R
|
|
|
Submission date |
Apr 09, 2009 |
Last update date |
Dec 19, 2012 |
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 |
GPL6887 |
Series (1) |
GSE15616 |
Increased antigen cross-presentation but impaired cross-priming after activation of PPARĪ³ |
|