Nöhammer G
Institut für Biochemie, Karl-Franzens-Universität Graz, Austria.
Histochemistry. 1989;90(6):465-73. doi: 10.1007/BF00494358.
Previous methods for the histochemical demonstration of DNA were optimized. p-Toluene sulfonic acid as catalyst for hydrazone formation between the aldehydes generated after Feulgen hydrolysis and 3-hydroxy-2-naphthoic acid hydrazide (NAH) was used instead of acetic acid. Modifications of the conditions of the coupling reaction with Fast Blue B reduced the background staining. The optimized histochemical staining method for DNA (NAH-FB-DNA staining) can be performed easily and reproducibly. Without prior Feulgen hydrolysis the optimized method can also be used for the histochemical demonstration of reactive carbonyls undissolved under the given histochemical conditions.
对先前用于DNA组织化学显示的方法进行了优化。用对甲苯磺酸作为Feulgen水解后产生的醛与3-羟基-2-萘酰肼(NAH)之间腙形成反应的催化剂,取代了乙酸。用固蓝B对偶联反应条件进行的修改减少了背景染色。优化后的DNA组织化学染色方法(NAH-FB-DNA染色)操作简便且可重复。在不进行预先Feulgen水解的情况下,该优化方法还可用于组织化学显示在给定组织化学条件下不溶解的活性羰基。