Application of Real Time PCR for the Quantitative Detection of Radiation-induced Genomic DNA Strand Breaks
-
- Yamauchi Emiko
- Division of Radiological Protection and Biology, National Institute of Infectious Diseases Department of Biological Production, Tokyo University of Agriculture and Technology
-
- Watanabe Ritsuko
- Radiation Effect Analysis Group, Japan Atomic Energy Agency
-
- Oikawa Miyoko
- Division of Radiological Protection and Biology, National Institute of Infectious Diseases Division of Science and Technology, Shinshu University
-
- Fujimoto Hirofumi
- Division of Radiological Protection and Biology, National Institute of Infectious Diseases
-
- Yamada Akinori
- Center of Molecular Biosciences, University of Ryukyus
-
- Saito Kimiaki
- Radiation Effect Analysis Group, Japan Atomic Energy Agency
-
- Murakami Masahiro
- Radiation Hazard Research Group, National Institute of Radiological Sciences
-
- Hashido Kazuo
- Division of Radiological Protection and Biology, National Institute of Infectious Diseases
-
- Tsuchida Kozo
- Division of Radiological Protection and Biology, National Institute of Infectious Diseases
-
- Takada Naoko
- Division of Radiological Protection and Biology, National Institute of Infectious Diseases
-
- Fugo Hajime
- Department of Biological Production, Tokyo University of Agriculture and Technology
-
- Tu Zhenli
- College of Animal Sciences, Zhejiang University
-
- Maekawa Hideaki
- Division of Radiological Protection and Biology, National Institute of Infectious Diseases
この論文をさがす
説明
The frequency of single strand breaks (SSBs) occurring on both strands of the pBR322 plasmid DNA region flanked by a pair of primers used for polymerase chain reaction (PCR) amplifications was determined after irradiation with 137Cs γ rays. We verified that real time PCR is suitable for the detection and quantitative analysis of SSBs caused by γ ray irradiation. The utility of this approach was also supported by the comparison of the practical experimental data with the Monte Carlo simulation. The potential application of this PCR method for the detection of genomic DNA damage was also confirmed.<br>
収録刊行物
-
- Journal of Insect Biotechnology and Sericology
-
Journal of Insect Biotechnology and Sericology 77 (1), 1_17-1_24, 2008
社団法人 日本蚕糸学会
- Tweet
キーワード
詳細情報 詳細情報について
-
- CRID
- 1390282680173907712
-
- NII論文ID
- 10021220872
-
- NII書誌ID
- AA11558849
-
- ISSN
- 18847978
- 13468073
-
- NDL書誌ID
- 9400339
-
- 本文言語コード
- en
-
- データソース種別
-
- JaLC
- NDL
- CiNii Articles
-
- 抄録ライセンスフラグ
- 使用不可