| Project/Area Number |
23561012
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Nuclear engineering
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| Research Institution | Osaka University |
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Principal Investigator |
SHIMIZU Kikuo 大阪大学, ラジオアイソトープ総合センター, 准教授 (20162696)
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| Co-Investigator(Kenkyū-buntansha) |
IIDA Toshiyuki 大阪大学, 大学院工学研究科, 教授 (60115988)
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| Project Period (FY) |
2011 – 2013
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| Project Status |
Completed (Fiscal Year 2013)
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| Budget Amount *help |
¥5,460,000 (Direct Cost: ¥4,200,000、Indirect Cost: ¥1,260,000)
Fiscal Year 2013: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2012: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2011: ¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
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| Keywords | DNA線量計 / 個人被ばく線量 / LET / リアルタイムPCR / 被ばく評価 / 米国 / 英国 / PCR / バイオドシメトリ / DNA損傷 / 吸収線量 |
|---|
| Research Abstract |
The biological dosimeter that measures biological responses to ionizing radiation is useful for radiation protection. We report the development and characterization of a gamma-ray irradiation dosimetry system based on Real-time PCR methodology. Real-time PCR is used to amplify and simultaneously quantify a targeted DNA molecule. If there are no limitations due to limiting substrates or reagents, at each extension step, the amount of DNA target is doubled, leading to exponential amplification of the specific DNA fragment. The essential point of this assay is that DNA lesions caused by ionizing radiation block DNA synthesis by DNA polymerase, resulting in a decrease in the amplification of a damaged DNA template compared with that of non-damaged DNA templates.
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