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Status |
Public on Aug 10, 2016 |
Title |
1051 |
Sample type |
RNA |
|
|
Source name |
Nrf2 knockout (+1/+1) /Vehicle
|
Organism |
Rattus norvegicus |
Characteristics |
strain: F344 genotype/variation: Nrf2 knockout (+1/+1) tissue: liver treatment: Vehicle
|
Treatment protocol |
Gavage of CDDO-Im (30 umol/kg body weight, 6 hours)
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted from whole livers using Sepazol-RNA I Suger G (Nacalai Tesque).
|
Label |
Cy3
|
Label protocol |
500 ng of total RNA was amplified and labeled using the Agilent Low RNA Input Fluorescent Linear Amplification Kit according to the manufacturer's protocol.
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|
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Hybridization protocol |
1.65 ug of Cy3-labeled cRNA were mixed and fragmented using the Agilent In Situ Hybridization Kit protocol. Hybridizations were performed for 16 hours in a rotating hybridization oven according to the Agilent 60-mer oligo microarray processing protocol prior to washing.
|
Scan protocol |
Slides were scanned with an Agilent DNA Microarray Scanner model G2539.
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Description |
Gene expression in Vehicle-treated Nrf2 knockout (+1+1) rat
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Data processing |
Data was obtained using the Agilent Feature Extraction software (v10.1), using default for all parameters. The data were analyzed using GeneSpring GX software (v11.5) (Agilent).
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|
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Submission date |
Jan 29, 2016 |
Last update date |
Aug 10, 2016 |
Contact name |
Keiko Taguchi |
E-mail(s) |
[email protected]
|
Organization name |
Tohoku University
|
Department |
Graduate School of Medicine
|
Lab |
Medical Biochemistry
|
Street address |
2-1 Seiryo-cho, Aoba
|
City |
Sendai |
State/province |
Miyagi |
ZIP/Postal code |
980-8575 |
Country |
Japan |
|
|
Platform ID |
GPL14746 |
Series (1) |
GSE77377 |
Comparison of gene expression profiles of wildtype and two lines of Nrf2 knockout rat livers with or without CDDO-Im treatment |
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