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Status |
Public on Aug 10, 2016 |
Title |
iTreg_rep2 |
Sample type |
RNA |
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Source name |
Treg, IVIg-induced
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Organism |
Mus musculus |
Characteristics |
tissue: spleen cell type: T lymphocyte
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Treatment protocol |
Spleens were dissected, lymphocytes were prepared, and Treg were isolated by flow cytometric sorting.
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Growth protocol |
DEREG mice were sensitized and challenged with ovalbumin (OVA) to induce allergic airways disease. Endogenous Treg were depleted with injection of 40 ng/g diptheria toxin before IVIg or HSA treatment (2 g/kg).
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Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with TRIzol reagent (Life Technologies) and cleaned with RNeasy Mini silica-gel membrane columns (Qiagen).
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Label |
biotin
|
Label protocol |
2 ng of total RNA were subjected to two rounds of amplification using Affymetrix GeneChip Pico WT two-cycle target labeling and control reagents according to the manufacturer's protocols
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Hybridization protocol |
Following fragmentation, target ss-DNA was hybridized for 16 hours at 45°C to Affymetrix Mouse Gene 2.0 ST arrays. Arrays were stained and washed using the GeneChips Fluidics Station 450.
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Scan protocol |
Arrays were scanned on an Affymetrix GeneChip Scanner 3000 7G. Images were processed using GeneChip Command Console (AGCC) software to generate CEL files.
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Description |
Gene expression data of IVIg-generated induced Treg from allergen-exposed IVIg-treated animals
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Data processing |
Raw data was read using the Bioconductor oligo package. Probe intensities were normalized across all arrays by the robust multi-array average (RMA) algorithm.
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Submission date |
Aug 06, 2015 |
Last update date |
Aug 10, 2016 |
Contact name |
Bruce David Mazer |
E-mail(s) |
bruce.mazer@mcgill.ca
|
Organization name |
RI-MUHC
|
Department |
RESP
|
Street address |
1001 boul. Décarie
|
City |
Montreal |
State/province |
Quebec |
ZIP/Postal code |
H4A 3J1 |
Country |
Canada |
|
|
Platform ID |
GPL16570 |
Series (1) |
GSE71811 |
Gene expression data from mouse regulatory T cells |
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