|
Status |
Public on Aug 04, 2008 |
Title |
jurkat_rep1 |
Sample type |
RNA |
|
|
Source name |
Jurkat cells rep 1
|
Organism |
Homo sapiens |
Characteristics |
Jurkat, Human T-acute lymphoblastic leukemia
|
Biomaterial provider |
ATCC
|
Treatment protocol |
Allowed to reach 6 X 10 5 cells/ml.
|
Growth protocol |
RPMI-1640 (Mediatech), 10% FBS (Gibco), 2mmol/L L-glutamine (Mediatech), 100IU/ml penicillin, 100 microgram/ml streptomycin, 0.25 microgram/ml amphotericin B (all from Mediatech) at 37 degrees Celsius, 5% carbon dioxide, 95% air, and 80% relative humidity.
|
Extracted molecule |
total RNA |
Extraction protocol |
Trizol
|
Label |
biotin
|
Label protocol |
IVT Labeling Affymetrix
|
|
|
Hybridization protocol |
GeneChip Hybridization oven 640
|
Scan protocol |
GeneChip Scanner
|
Description |
Jurkat cells are an immortalized line of T lymphocyte cells that are used to study acute T cell leukemia. The cell line was established from peripheral blood of a human with T cell leukemia.
|
Data processing |
MAS5.0
|
|
|
Submission date |
Nov 20, 2007 |
Last update date |
Aug 28, 2018 |
Contact name |
Nathan J. Bowen |
E-mail(s) |
nbowen@cau.edu
|
Phone |
4048808158
|
Organization name |
Clark Atlanta University
|
Department |
Center for Cancer Research and Therapeutic Development
|
Lab |
Cancer Development and Evolution
|
Street address |
223 James P Brawley Drive
|
City |
Atlanta |
State/province |
GA |
ZIP/Postal code |
30314 |
Country |
USA |
|
|
Platform ID |
GPL570 |
Series (1) |
GSE9648 |
Anticancer metabolites discovered by Computational Metabolomics |
|
Relations |
Reanalyzed by |
GSE119087 |