Abstract
DNA arrays, on which PCR products with various lengths were immobilized, were fabricated for identification of transcription factor binding site. Surface plasmon resonance (SPR) imaging technique ware applied to detect the bindings between an antioxidant sequence nqo1ARE and transcription factor Nrf2/MafG heterodimer.
Original language | English |
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Pages | 2069 |
Number of pages | 1 |
Publication status | Published - 2006 |
Event | 55th SPSJ Annual Meeting - Nagoya, Japan Duration: 2006 May 24 → 2006 May 26 |
Conference
Conference | 55th SPSJ Annual Meeting |
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Country/Territory | Japan |
City | Nagoya |
Period | 06/5/24 → 06/5/26 |
Keywords
- dsDNA arrays
- Heterobifunctional hydrophilic crosslinker
- PCR products
- Signal normalization
- Surface plasmon resonance (SPR) imaging technique
- Transcription factor binding site