|
Status |
Public on Jun 23, 2010 |
Title |
BDC Treg #2 |
Sample type |
RNA |
|
|
Source name |
T cells were sorted from the spleen of BDC2.5 RAG+/o NOD without treatment
|
Organism |
Mus musculus |
Characteristics |
strain: NOD genotype/variation: BDC2.5 TCR tg RAG1+/o Foxp3GFP NOD age: 28 days old number of mice per chip: one gender: female tissue: spleen cell type: B220-, CD8a-, CD11b/c-, CD4+,GFP+ T cells protocol: no treatment
|
Treatment protocol |
Anti-CD3 treatment (37.5 ug of anti-CD3 mAb (clone:KT3) was iv injected for 5 consecutive days from 17 days of age) or no treatment.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA isolated with Trizol reagent and amplified twice with the MessageAmp aRNA Kit (Ambion)
|
Label |
biotin
|
Label protocol |
Biotin
|
|
|
Hybridization protocol |
Biotin-labeled cRNA was fragmented and hybridized to the array in a cocktail containing control oligos at 45°C for 16 hours, rotated at 60rpm, in the Affymetrix GeneChip Hybridization Oven 640. After hybridization, the arrays were automatically cycled through buffer washes and stained with streptavidin R-phycoerythrin conjugate (Invitrogen) in the Affymetrix GeneChip Fluidics Station 400 (EukGE-WS2v4 protocol).
|
Scan protocol |
After staining and washing, the arrays were scanned in the Affymetrix GeneChip Scanner 3000 using the Affymetrix GCOS (GeneChip Operating Software) to automatically generate .CEL files.
|
Description |
jos4621.CEL
|
Data processing |
Raw data were preprocessed with the RMA algorithm in GenePattern, and averaged expression values were used for analysis.
|
|
|
Submission date |
Jun 23, 2010 |
Last update date |
Jun 23, 2010 |
Contact name |
CBDM Lab |
E-mail(s) |
cbdm@hms.harvard.edu
|
Phone |
617-432-7747
|
Organization name |
Harvard Medical School
|
Department |
Microbiology and Immunobiology
|
Lab |
CBDM
|
Street address |
77 Avenue Louis Pasteur
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02215 |
Country |
USA |
|
|
Platform ID |
GPL1261 |
Series (1) |
GSE22527 |
Anti-CD3 therapy permits regulatory T cells to surmount T cell receptor-specified peripheral niche constraints |
|