Lu L J, Tasaka F, Hokanson J A, Kohda K
Division of Environmental Toxicology, University of Texas Medical Branch, Galveston 77550.
Chem Pharm Bull (Tokyo). 1991 Jul;39(7):1880-2. doi: 10.1248/cpb.39.1880.
Using synthesized 8-hydroxy-2'-deoxyguanosine 3'-monophosphate as a marker, the 32P-postlabeling method was adapted with minimum modifications for the analysis of 8-hydroxy-2'-deoxyguanosine (8-OH-dG) content in deoxyribonucleic acid (DNA). This method allows the analysis of one 8-OH-dG per 10(4) DNA nucleotides with only 10 pmoles of nucleotides required. The amounts of 8-OH-dG in DNA detected by the postlabeling method correlated well with the electrochemical detection method but were consistently lower.
以合成的8-羟基-2'-脱氧鸟苷3'-单磷酸为标记物,对32P后标记法进行了最小程度的修改,以分析脱氧核糖核酸(DNA)中8-羟基-2'-脱氧鸟苷(8-OH-dG)的含量。该方法每10(4)个DNA核苷酸只需10皮摩尔核苷酸就能分析一个8-OH-dG。后标记法检测到的DNA中8-OH-dG的量与电化学检测法相关性良好,但始终较低。