|
Status |
Public on Oct 14, 2017 |
Title |
C14_12h_con_repC |
Sample type |
RNA |
|
|
Source name |
CEM C7-14_12h_ethanol
|
Organism |
Homo sapiens |
Characteristics |
cem clone id: CEM C7-14 cell type: human leukemic cells time: 12h treatment: ethanol
|
Treatment protocol |
Dex in ethanol was added to 10E-6 M Dex and <1% ethanol final. Control cultures received ethanol only.
|
Growth protocol |
CEM cells were maintained in log growth till the initiation of treatment. Triplicate independent cultures were then placed in tissue culture wells at 2x10E5 cells per ml. growth medium.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted from concentrated, washed cells by use of Qiagen RNA isolaztion kit.
|
Label |
biotin
|
Label protocol |
RNA was biotin labeled by use of ENZO Biochem. Trascriptional labeling kit.
|
|
|
Hybridization protocol |
Post fragmentation, hybridization was carried out as described (RD Medh, et al. Genomics 2003. 81(6):543-55
|
Scan protocol |
Gene Array Scanner (Hewlet Packard)
|
Description |
12hGCC-14con
|
Data processing |
By Affymetrix Gene Chip Suites 4.0 and 5.0 (the latter in Gene Spring software version 4.2.1)
|
|
|
Submission date |
Oct 13, 2017 |
Last update date |
Oct 14, 2017 |
Contact name |
Scott Andrew Ochsner |
E-mail(s) |
sochsner@bcm.edu
|
Phone |
713-798-6227
|
Organization name |
Baylor College of Medicine
|
Department |
Molecular and Cellular Biology
|
Lab |
SPP: Signaling Pathways Project
|
Street address |
One Baylor Plaza
|
City |
Houston |
State/province |
TX |
ZIP/Postal code |
77030 |
Country |
USA |
|
|
Platform ID |
GPL8300 |
Series (2) |
GSE104930 |
Sequential gene regulatory events leading to glucocorticoid-evoked apoptosis of CEM human leukemic cells [HG_U95Av2] |
GSE104932 |
Sequential gene regulatory events leading to glucocorticoid-evoked apoptosis of CEM human leukemic cells |
|