van Ingen E M, Tanke H J, Ploem J S
J Histochem Cytochem. 1979 Jan;27(1):80-3. doi: 10.1177/27.1.571445.
The specificity and quantitative reliability of the Feulgen-acriflavine-SO2 procedure was tested on polyacrylamide model films containing DNA. Noncovalent binding of acriflavine to DNA was observed when the washing procedure, as used in the classical way, was applied. The noncovalently bound acriflavine could be removed with an extra wash in acid-ethanol. The presence of SO2 in the staining solution has been found to enhance covalent binding significantly. The absorbance of films stained by our Feulgen-acriflavine-SO2 procedure is directly proportional to that obtained by the classical Feulgen-pararosanilline-SO2 procedure. The acriflavine-Feulgen procedure has also been tested using a commercial and a purified dye. The use of purified acriflavine, compared to a commercial sample did not result in a significant difference in the maximum absorbance value of stained DNA nor in the absorption or the fluorescence emission spectra of acriflavin covalently bound to DNA.
在含有DNA的聚丙烯酰胺模型膜上测试了福尔根-吖啶黄-SO₂ 法的特异性和定量可靠性。当采用经典方法中的洗涤步骤时,观察到吖啶黄与DNA的非共价结合。通过在酸乙醇中额外洗涤,可以去除非共价结合的吖啶黄。已发现染色溶液中SO₂ 的存在可显著增强共价结合。用我们的福尔根-吖啶黄-SO₂ 法染色的膜的吸光度与经典福尔根-副品红-SO₂ 法获得的吸光度成正比。还使用市售染料和纯化染料测试了吖啶黄-福尔根法。与市售样品相比,使用纯化的吖啶黄在染色DNA的最大吸光度值、与DNA共价结合的吖啶黄的吸收光谱或荧光发射光谱方面均未产生显著差异。