|
Status |
Public on Mar 31, 2011 |
Title |
Th1 |
Sample type |
RNA |
|
|
Source name |
primary CD4 T cells from spleen
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6 tissue: spleen cell type: CD4 T cell culture conditions: Th1
|
Treatment protocol |
Th1 and Th2 culture cells were collected and resuspendet in the Trizol solution (GibcoBRL).
|
Growth protocol |
Splenic CD4 T cells were prepared using a magnetic cell sorter (AutoMACS; Miltenyi Biotec) yielding a purity of >98%. Where indicated, cells from C57BL/6 mice were stimulated with immobilized anti-TCR mAb (H57−597; 3 mg/ml) and anti-CD28 mAb under Th1- or Th2-culture conditions for 2days in vitro. Th1 conditions; 25 U/ml IL-2, 10 U/ml IL-12, and antiミIL-4 mAb. Th2 conditions; 25 U/ml IL-2, 100 U/ml IL-4. pMX-IRES-NGFR retrovirus were added to the Th1 and Th2 cell differentiation cultures on day 2. After culturing for 3 more days, the cells were harvested.
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol extraction of total RNA was performed according to the manufacturer's instructions.
|
Label |
biotin
|
Label protocol |
Total RNA was extracted using the IVT Labeling kit from Affymetrix
|
|
|
Hybridization protocol |
aRNA was hybridized to GeneChip Mouse Genome 430 2.0 Arrays from Affymetrix according the manufacturers protocol.
|
Scan protocol |
GeneChips were scanned using the GeneChip Scanner 3000.
|
Description |
Gene expression data from wild type CD4+ T cells cultured for 5 days in Th1 condition
|
Data processing |
Expression values were determined using GeneChip Operating Software (GCOS) v1.2 software.
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|
|
Submission date |
Mar 31, 2011 |
Last update date |
Aug 04, 2011 |
Contact name |
Atsushi Onodera |
Organization name |
Chiba University
|
Department |
Immunology
|
Street address |
Chuo-ku Inohana 1-8-1
|
City |
Chiba |
ZIP/Postal code |
260-8670 |
Country |
Japan |
|
|
Platform ID |
GPL1261 |
Series (1) |
GSE28292 |
Genome-wide analysis reveals unique regulation of transcription of Th2-specific genes by GATA3 |
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