DNA-benzoquinone adducts analyzed by nuclease P1 m ediated 32P-postlabeling method |
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作者姓名: | Jiang Xiangning Liu Sufen Xu Xiaobai |
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作者单位: | Research Center for Eco-Environmental Sciences,Chinese Academy of Sciences,Beijing 100085,China,Research Center for Eco-Environmental Sciences,Chinese Academy of Sciences,Beijing 100085,China,Research Center for Eco-Environmental Sciences,Chinese Academy of Sciences,Beijing 100085,China |
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摘 要: | With the super high sensitivity,high reproducibility and accumcy,nuclease P1 mediated 32P-postlabeling version has been successfully used to analyze the DNA-benzoquinone(DNA-BQ)adducts formed from m vitro cultured cells,reaction of benzoquinone ith calf thymus DNA and nucleoside monophosphates.It has been proven that the maior radioactive spot,contributing more than 70% of the total radioactivity of DNA-BQ adducts detected,is from deoxycytidine(dC)modified by benzoqumone while a minor one from deoxyguanosme(dGl.The method is capable of detecting 1 adduct in 109 to 1010 DNA bases.
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关 键 词: | P1 mediated 32p-postlabelmg;DNA-BQ adducts;dC-BQ adduct;dG-BQ adduct |
收稿时间: | 1991-09-16 |
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