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Status |
Public on Apr 01, 2011 |
Title |
Gene expression in NRF2-knockdown A549 cells (no.2) |
Sample type |
RNA |
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Source name |
human lung cancer cell line, A549 cells, treated with NRF2 siRNA (HSS107129)
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Organism |
Homo sapiens |
Characteristics |
treatment: NRF2 KD-2 cell line: A549
|
Treatment protocol |
The siRNAs were introduced into A549 cells by electroporation using the MP-100 MicroPorator (Digital Bio Technology).
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Growth protocol |
A549 cells were maintained in RPMI1640 medium supplemented with 20% FBS.
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Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted from A549 cells using Isogen (Nippon Gene). RNA was further purified using an RNeasy Mini Kit (Qiagen).
|
Label |
Cy3
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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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Hybridization protocol |
750 ng of Cy3-labeled cRNA was 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.
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Scan protocol |
Slides were scanned with an Agilent DNA Microarray Scanner model G2539.
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Description |
Gene expression at 24 hours after transfection
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Data processing |
Agilent Feature Extraction Software
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Submission date |
Mar 29, 2011 |
Last update date |
Apr 07, 2011 |
Contact name |
Hozumi Motohashi |
E-mail(s) |
hozumim@med.tohoku.ac.jp
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Phone |
81-22-717-8087
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Fax |
81-22-717-8090
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Organization name |
Tohoku University Graduate School of Medicine
|
Department |
Center for Radioisotope Science
|
Street address |
2-1 Seiryo-machi, Aoba-ku
|
City |
Sendai |
State/province |
Miyagi |
ZIP/Postal code |
980-8575 |
Country |
Japan |
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Platform ID |
GPL4133 |
Series (1) |
GSE28230 |
Comparison of gene expression profiles of A549 cell treated with NRF2 siRNA and control siRNA |
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