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Status |
Public on Feb 09, 2017 |
Title |
SLE DCs Replicate 1 |
Sample type |
RNA |
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Source name |
monocyte-derived DCs
|
Organism |
Homo sapiens |
Characteristics |
diagnosis: systemic lupus erythematosus tissue: PBMC age: day7 cell type: dendritic cells
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Growth protocol |
PBMC were isolated and monocyte-derived dendritic cells were sorted by positive selection of CD14+ monocytes using magnetic beads. The cells were then cultured for 5-7 days supplemented with GM-CSF and IL-4. For DC maturation, 1μg/ml LPS was added to the medium at day 6.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA extracted using Trizol following manufacturer's instructions
|
Label |
Cy3
|
Label protocol |
Total RNA was amplified using the Low Input Quick Amp WT Labeling kit, according to the manufacturer’s instructions (Agilent Technologies, Santa Clara, USA). 100 ng of total RNA was reverse-transcribed into double-stranded cDNA, which was translated into cRNA in the presence of Cy3-dCTP and amplified by T7 RNA polymerase.
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Hybridization protocol |
Oligoarray control targets and hybridization buffer (Agilent In Situ Hybridization Kit Plus) were added, and samples were applied to microarrays enclosed in Agilent SureHyb-enabled hybridization chambers. After hybridization, slides were washed sequential
|
Scan protocol |
Microarray images were acquired using an Agilent DNA microarray scanner.
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Data processing |
Agilent Feature Extraction Software (V10.7) was used for background subtraction and Quantile normalization.
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Submission date |
Mar 15, 2016 |
Last update date |
Feb 09, 2017 |
Contact name |
Yilun Wang |
E-mail(s) |
yolendawang@163.com
|
Organization name |
Fudan University
|
Street address |
No.12 Wulumuqi Zhong Road
|
City |
Shanghai |
ZIP/Postal code |
200040 |
Country |
China |
|
|
Platform ID |
GPL18402 |
Series (1) |
GSE79240 |
microRNA profilling in dendritic cells of systemic lupus erythematosus |
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