|
Status |
Public on Jul 28, 2014 |
Title |
Donor BB - HIN1 - 4 HAU/ml - mAdbID:111301 |
Sample type |
RNA |
|
|
Channel 1 |
Source name |
Pooled PBMC Reference
|
Organism |
Homo sapiens |
Characteristics |
tissue: blood cell type: peripheral blood mononuclear cells (PBMCs) other: Sample Pooling Protocol: A pool of total RNA derived from independent human PBMCs served as a common reference.
|
Extracted molecule |
total RNA |
Extraction protocol |
Sample Extraction Protocol Other: Total RNA was isolated from virus-stimulated samples and untreated controls with Qiagen RNeasy Plus microkits (Qiagen, Valencia, CA).
|
Label |
cy3
|
Label protocol |
Cy3 Sample Labeling Other: Samples were directly labeled with the Kreatech (Durham, NC) ULS aRNA fluorescent labeling kit.
|
|
|
Channel 2 |
Source name |
Donor BB - H1N1 - 4 HAU/ml
|
Organism |
Homo sapiens |
Characteristics |
tissue: blood cell type: Plasmacytoid dendritic cells (pDCs) individual: Donor BB
|
Treatment protocol |
Treatment dose: 4 HAU/ml Treatment time: 6 hours In-vitro treatment: Human plasmacytoid dendritic cells (pDCs) were isolated by negative selection from PBMCs of healthy blood donors and cultured for 18 hours prior to infection. pDCs were stimulated for 6 hours with influenza virus A/PR/8/34 (H1N1; Charles River Laboratories) at 4 HAU/ml.
|
Extracted molecule |
total RNA |
Extraction protocol |
Sample Extraction Protocol Other: Total RNA was isolated from virus-stimulated samples and untreated controls with Qiagen RNeasy Plus microkits (Qiagen, Valencia, CA).
|
Label |
cy5
|
Label protocol |
Cy5 Sample Labeling Other: Samples were directly labeled with the Kreatech (Durham, NC) ULS aRNA fluorescent labeling kit.
|
|
|
|
Hybridization protocol |
Hybrization Protocol Other: Hybridization was carried out in a water bath at 42C for 18 hours.
|
Scan protocol |
Scan_MicronsPerPixelX: 10 Scan_MicronsPerPixelY: 10 Scan_ScannerName: Agilent Technologies Scanner G2505B US45103062
|
Description |
mAdb experiment ID: 111301
|
Data processing |
Agilent Data Processing Protocol Calculation Method: Images were auto gridded, analyzed and data extracted using Agilent Feature Extraction Software. Spot values were normalized using the default linear-lowess normalization. FeatureExtractor_Version: 9.5.1.1 Protocol_Name: GE2-NonAT_95_Feb07 (Read Only)
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|
|
Submission date |
Jul 28, 2014 |
Last update date |
Jul 28, 2014 |
Contact name |
Francesco Maria Marincola |
E-mail(s) |
[email protected]
|
Phone |
301-793-8210
|
Organization name |
Sidra Medical and Research Center
|
Street address |
Al Nasr Tower, AL Corniche Street, PO Box 26999
|
City |
Doha |
ZIP/Postal code |
PO Box 26999 |
Country |
Qatar |
|
|
Platform ID |
GPL7088 |
Series (1) |
GSE59837 |
Differential Responses of Plasmacytoid Dendritic Cells to Influenza and Distinct Viral Pathogens |
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