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Status |
Public on Apr 30, 2023 |
Title |
Virus_infected cells, biological rep1 |
Sample type |
RNA |
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Source name |
Canine alveolar macrophage
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Organism |
Canis lupus familiaris |
Characteristics |
breed: beagle cell type: canine alveolar macrophages (CAMCs) infection: H3N2 canine influenza virus (CIV) JS/10
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Treatment protocol |
Primary CAMCs were seeded onto sterile 24-well plates at a density of 2×105 cells/well, infected with JS/10 or phosphate buffered saline (PBS).
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Growth protocol |
Primary canine alveolar macrophages (CAMCs) were obtained from broncho-alveolar lavage (BAL) of beagle dog and cultured at 37 °C under 5% CO2 atmosphere.
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted from 1×10e6 cells of primary CAMCs infected and mock-infected with JS/10 for 24 h using TRIzol reagent (Invitrogen, New York, USA). RNA samples were spectroscopically verified for purity, quality of the intact RNA without genomic DNA contamination was assessed using an Agilent 2100 Bioanalyzer.
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Label |
biotin
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Label protocol |
Biotinylated cRNA were prepared according to the standard Affymetrix protocol.
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|
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Hybridization protocol |
Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Canine Genome 2.0 Array.
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Scan protocol |
GeneChips were scanned using an Affymetrix GCS 3000 7G Scanner.
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Description |
Expression data from canine alveolar macrophages
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Data processing |
The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method.
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Submission date |
May 01, 2020 |
Last update date |
Apr 30, 2023 |
Contact name |
Maoda Pang |
E-mail(s) |
pangmaoda@jaas.ac.cn
|
Organization name |
Nanjing Agricultural University
|
Street address |
NO.1 Zhongling Street
|
City |
Nanjing |
ZIP/Postal code |
210000 |
Country |
China |
|
|
Platform ID |
GPL21572 |
Series (1) |
GSE149700 |
Expression data from canine alveolar macrophages |
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