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Status |
Public on Aug 02, 2007 |
Title |
2nd MPSS library produced from activated CD4+ T cell clone 29 |
Sample type |
MPSS |
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Source name |
human CD4+ T cell clone 29
|
Organism |
Homo sapiens |
Characteristics |
CD4+ T cell clone 29 derived from PBMC from subject Immunogen: MVA virus containing HIV-1 gag gene Peptide Specificity: KRWIILGLNKVIRMY TCR usage: Vbeta17
|
Treatment protocol |
T cells were activated with beads coated in monoclonal antibodies specific for CD3 and CD28.
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Growth protocol |
The clone was established in culture with IL-7 and the HIV-1 gag peptides KRWIILGLNKVIRMY and GEIYKRWIILGLNKI (but later shown to be specific for the former)
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted from T cells using Trizol according to standard methods and sent to Lynx therpeutics for the generation and sequencing of an MPSS library.
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Description |
2nd MPSS library produced from a single sample of RNA from an activated CD4+ T-cell clone.
|
Data processing |
Data file includes simply the tags identified and their counts in the library
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|
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Submission date |
Jul 27, 2007 |
Last update date |
Aug 01, 2007 |
Contact name |
Edward J Evans |
E-mail(s) |
edward.evans@ndm.ox.ac.uk
|
URL |
http://www.t-cellbiology.org
|
Organization name |
University of Oxford
|
Department |
Nuffield Dept. Clinical Medicine
|
Lab |
T-cell Biology Group
|
Street address |
HIU, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital
|
City |
Oxford |
State/province |
Oxfordshire |
ZIP/Postal code |
OX3 9DS |
Country |
United Kingdom |
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|
Platform ID |
GPL5678 |
Series (1) |
GSE8612 |
SAGE and MPSS libraries from activated CD4+ T cell clone 29 |
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