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Status |
Public on Jun 24, 2006 |
Title |
GFP_YOUNG_HD1_REP2 |
Sample type |
RNA |
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|
Source name |
CD8 T lymphocytes
|
Organism |
Homo sapiens |
Characteristics |
early passage CD8 T cells expressing GFP.
|
Treatment protocol |
Mycoplasma-free cells were harvested after 15 to 18 days of mitogen stimulation (PHA), Annexin-V expression <10%.
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Growth protocol |
Cell are cultures in RPMI 1640 medium supplemented with 8% Human Serum and 150U/ml of rIL-2 (GlaxoSmithKline) and stimulated using PHA (Sodiag) and irradiated feeder cells.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA from 30x10E6 cells was extracted, purified and used for cDNA synthesis following standard procedures (www.Affymetrix.com).
|
Label |
biotin
|
Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 2.5 micrograms total RNA.
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|
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Hybridization protocol |
Following fragmentation, 10 micrograms of cRNA were hybridized for 16 hr on human U133A GeneChip, Chips were washed and stained in the Fluidics Station 400.
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Scan protocol |
GeneChips were scanned using the Hewlett-Packard GeneArray Scanner.
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Description |
GFP expressing transduced CD8 T Lymphocytes, early passage, healthy donor 1, rep2
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Data processing |
The .cel files data were analyzed with the R library affy, using RMA default settings and the quantile normalization method.
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Submission date |
Jun 23, 2006 |
Last update date |
Jun 23, 2006 |
Contact name |
Mauro Delorenzi |
E-mail(s) |
[email protected]
|
Organization name |
Swiss Institute of Bioinformatics
|
Lab |
BCF
|
Street address |
GĂ©nopode Building, Quartier Sorge
|
City |
Lausanne |
ZIP/Postal code |
1015 |
Country |
Switzerland |
|
|
Platform ID |
GPL96 |
Series (2) |
GSE5142 |
hTERT effects in CD8 T Lymphocytes HD1 |
GSE5144 |
hTERT effects in CD8 T Lymphocytes from two healthy donors |
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