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Status |
Public on May 12, 2016 |
Title |
M1-BMDMs_WT_replicate1 |
Sample type |
RNA |
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Source name |
BMDMs, WT, LPS and IFNg, 6hrs, replicate1
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6 gender: Male age: 8 weeks cell type: BMDM genotype/variation: WT treatment: M1-stimuli (LPS and IFNg)
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Treatment protocol |
BMDMs are untreated, or treated with M1-stimuli (LPS and IFNg) or with M2-stimuli (IL-4) for 6 hours.
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Growth protocol |
Bone marrow cells were cultured in DMEM supplemented with 10% fetal bovine serum, M-CSF, and Antibiotic-Antimycotic. The cultures were incubated at 37 ÂșC in a humidified incubator with 5% CO2 for 7 days.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted from BMDMs using RNeasy Micro kit (Qiagen).
|
Label |
Cy3
|
Label protocol |
RNA samples were labeled with Cy3 using the Quick Amp Labeling kit (Agilent) according to the manufacturer's protocol.
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Hybridization protocol |
Cy3-labeled cRNA were mixed and fragmented using the Agilent In Situ Hybridization Kit protocol. Hybridizations were performed for 16 hours according to the Agilent 60-mer oligo microarray processing protocol prior to washing.
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Scan protocol |
Slides were scanned with an Agilent DNA Microarray Scanner.
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Description |
Gene expression in wild-type BMDMs stimulated with LPS and IFNg for 6hrs, replicate1
|
Data processing |
The data were normalized by percentile shift and filtered by flag, using GeneSpring GX software (Silicon Genetics).
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Submission date |
Jul 23, 2015 |
Last update date |
May 12, 2016 |
Contact name |
Eri H Kobayashi |
Organization name |
Tohoku University Graduate School of Medicine
|
Department |
Medical Biochemistry
|
Street address |
2-1 Seiryo-machi, Aobaku
|
City |
Sendai |
State/province |
Miyagi |
ZIP/Postal code |
980-8575 |
Country |
Japan |
|
|
Platform ID |
GPL7202 |
Series (1) |
GSE71263 |
Nrf2 suppresses macrophage inflammatory response by blocking proinflammatory cytokine transcription |
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