|
Status |
Public on Oct 17, 2013 |
Title |
Bcell_activated_6hrs, AG2 |
Sample type |
RNA |
|
|
Source name |
Bcell, activated, 6hrs
|
Organism |
Homo sapiens |
Characteristics |
disease status: healthy cell type: B cells gp120 treatment: none time point: 6hrs
|
Treatment protocol |
Isolated B cells were treated with gp120 proteins of different affinity or mock protein. The exposure time points included 30min, 3hrs and 6hrs.
|
Growth protocol |
Freshly isolated PBMCs were obtained from healthy donors and separated by Ficoll-Hypaque. Purified CD4+ T cells or B cells were obtained by negative selection using magnetic beads (StemCell Technologies, Vancouver, Canada). Cultured CD4+ cells were activated with OKT3, IL2 (20IU/ml) and all-trans retinoic acid (RA, 10nM) unless otherwise specified. RA was obtained from Sigma (St. Louis, MO) and discarded 1 month after reconstitution.
|
Extracted molecule |
total RNA |
Extraction protocol |
cDNA of each sample was generated with Ambion WT Expression Kit.
|
Label |
biotin
|
Label protocol |
cRNA was labelled according to the manufacturer's recommended standard protocol for the Affymetrix Human Gene 1.0 ST microarray.
|
|
|
Hybridization protocol |
Labeled cRNA was hybridized to the Affymetrix Human Gene 1.0 ST microarray according to the manufacturer's recommended standard protocol.
|
Scan protocol |
Hybridized Affymetrix human gene microarrays were scanned according to the manufacturer's recommended standard protocol.
|
Description |
AG2
|
Data processing |
Gene expression profiles were analyzed using Partek Genomic Suite 6.6.
|
|
|
Submission date |
Jul 18, 2013 |
Last update date |
Sep 01, 2016 |
Contact name |
Richard Lempicki |
Organization name |
NCI-Frederick
|
Lab |
Laboratory of Immunopathogenesis and Bioinformatics
|
Street address |
1050 Boyles Street / P.O. Box B
|
City |
Frederick |
State/province |
MD |
ZIP/Postal code |
21702 |
Country |
USA |
|
|
Platform ID |
GPL6244 |
Series (1) |
GSE49019 |
HIV-1 gp120 impairs B cell proliferation by inducing TGF-β1 production and FcRL4 expression via an α4β7-dependent mechanism |
|
Relations |
Reanalyzed by |
GSE86357 |