|
Status |
Public on Dec 17, 2015 |
Title |
MDM-24h-dex100nM-rep3 |
Sample type |
RNA |
|
|
Source name |
monocyte derived macrophage
|
Organism |
Homo sapiens |
Characteristics |
source: fully anonymized volunteers cell type: monocyte derived macrophage time: 24h treatment: dex 100nM
|
Treatment protocol |
Samples were treated with 100nM dexamethasone (Sigma) for the indicated duration
|
Growth protocol |
CD14+ monocytes were extracted from whole blood donated by healthy volunteers using MACS separation (Miltenyi). They were differentiated in culture for 1 week in the presence of recombinant human CSF1 (10000U/ml),penicillin/streptomycin, Glutamax and 10% fetal calf serum then replated in fresh medium, also supplemented as above, for the time series experiment.
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted using the RNeasy kit (Qiagen) and quality assessed using an 2100 Bioanalyzer (Agilent )
|
Label |
biotin
|
Label protocol |
Standard affymetrix protocols, Performed by Edinburgh Genomics.
|
|
|
Hybridization protocol |
Standard affymetrix protocols using GeneTitan. Performed by Edinburgh Genomics.
|
Scan protocol |
Standard affymetrix protocols using GeneTitan. Performed by Edinburgh Genomics.
|
Data processing |
Raw data was processed using R/Bioconductor: arrayQualityMetrics for quality control and the rma algorithm in the affy package to generate expression values.
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|
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Submission date |
Sep 29, 2014 |
Last update date |
Dec 17, 2015 |
Contact name |
Alasdair W Jubb |
E-mail(s) |
alasdair.jubb@ed.ac.uk
|
Organization name |
University of Edinburgh
|
Department |
Roslin Institute
|
Lab |
Hume lab / Bickmore lab (MRC HGU)
|
Street address |
The Roslin Institute
|
City |
Easter Bush |
State/province |
Midlothian |
ZIP/Postal code |
EH25 9RG |
Country |
United Kingdom |
|
|
Platform ID |
GPL13158 |
Series (2) |
GSE61880 |
Expression response of human monocyte derived macrophages to dexamethasone over a 24h time series |
GSE61881 |
Divergent transcriptional activation by glucocorticoids in mouse and human macrophages is the result of gain and loss of enhancers |
|