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Sample GSM833306 Query DataSets for GSM833306
Status Public on May 03, 2012
Title wild type unstimulated replicate 2
Sample type RNA
 
Source name WT 2 medium
Organism Mus musculus
Characteristics treatment: unstimulated
cell type: bone-marrow derived dendritic cells
genetic background: C57Bl/6
genotype: Wild type
Treatment protocol Bone marrow-derived dendritic cells (BM-DCs) were transferred to new culture dishes at a density of 1 million BM-DC per 2 ml medium. The BM-DCs were incubated with either medium (unstimulated) or preformed Ag-Ab complexes (IC) containing 1 µg/ml OVA (Worthington) and 50 µg/ml rabbit anti-OVA IgG (ICN biomedicals) at 37 degrees for 4 hours.
Growth protocol Bone marrow was harvested from the femurs and tibia derived from two female and two male mice of each mouse strain. The cells of all 12 mice were cultured separately in IMDM supplemented with GM-CSF containing supernatant in petri dishes. Non-adherent and semi-adherent cells were transferred to new dishes and fresh medium on days 4 and 7. On day 10, the cells were harvested and the % of immature CD11c+ DCs was determined by flow cytometry, which was typically above 85%.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from cells by Qiagen RNA Easy kit. RNA was amplified by using the Illumina RNA Amplification kit.
Label Biotin
Label protocol Illumina RNA amplfication kit includes incorporation of biotin.
 
Hybridization protocol Samples were hybridised on Illumina mouse WG-6 V1.1 expression BeadChips.
Scan protocol BeadChips were scanned on the Illumina BeadArray 500GX Scanner.
Description 04_B
Data processing Raw data was exported by Illumina BeadStudio V3.0 software and imported and stored in Rosetta Resolver software.
Not Normalized data sheet contains intensities corrected for background by Rosetta's default error model; Normalized data sheet contains intensities normalized with Rosetta's default error model for Illumina arrays on a back-transformed linear scale and where different probes for the same gene are averaged and thus get the same value
 
Submission date Nov 15, 2011
Last update date May 03, 2012
Contact name Peter A.C. 't Hoen
E-mail(s) p.a.c.hoen@lumc.nl
Phone +31 71 5269421
Fax +31 71 5268285
URL http://www.humgen.nl
Organization name Leiden University Medical Center
Department Center for Human and Clinical Genetics
Street address PO Box 9600
City Leiden
ZIP/Postal code 2300 RC
Country Netherlands
 
Platform ID GPL6481
Series (1)
GSE33718 Genome-wide analysis of Fcγ receptor ligation on dendritic cells from wild-type, FcγRIIb KO or FcR γ chain KO mice

Data table header descriptions
ID_REF
VALUE intensities normalized with Rosetta's default error model for Illumina arrays on a back-transformed linear scale and where different probes for the same gene are averaged and thus get the same value

Data table
ID_REF VALUE
10243 0.18545
10280 0.06262
10575 0.11397
20048 0.11297
20296 31.12114
20343 0.42768
20373 0.07035
20431 43.38847
50014 0.02614
50017 1.02804
50019 0.75011
50020 0.20258
50022 0.01322
50025 0.0179
50026 0.33915
50035 0.15207
50037 0.34714
50039 2.26033
50040 0.49427
50041 0.7217

Total number of rows: 46643

Table truncated, full table size 764 Kbytes.




Supplementary data files not provided
Processed data included within Sample table
Processed data are available on Series record

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