Hemminki K, Försti A, Löfgren M, Segerbäck D, Vaca C, Vodicka P
Centre for Nutrition and Toxicology, Karolinska Institute, Huddinge, Sweden.
IARC Sci Publ. 1993(124):51-63.
The 32P-postlabelling technique involves many steps that need to be carefully controlled in order to obtain a reliable quantitative determination of DNA adducts. We have studied several of the parameters involved in the DNA digestion procedures as well as those concerned in the phosphorylation reaction. Since adducts behave in very different ways in the labelling reaction, an individual protocol has to be worked out for each particular type of adduct. Quantitation is usually possible only if a synthesized standard of the adduct under investigation is run in parallel to the DNA samples throughout the whole procedure.
32P后标记技术涉及许多步骤,为了可靠地定量测定DNA加合物,这些步骤需要仔细控制。我们研究了DNA消化程序以及磷酸化反应中涉及的几个参数。由于加合物在标记反应中的行为方式差异很大,因此必须针对每种特定类型的加合物制定单独的方案。只有在整个过程中与DNA样品平行运行所研究加合物的合成标准品时,通常才可能进行定量。