Curtis S K, Cowden R R
Histochemistry. 1983;78(4):503-11. doi: 10.1007/BF00496202.
Five basic fluorochromes were evaluated to determine whether or not any could be used in microfluorometric studies for the selective demonstration of nucleic acids. Only two of the fluorochromes - Nuclear Yellow (Hoechst 769121) and the phenoxyindole compound D261/37 - were found to be selective for nucleic acids, while the other three fluorochromes produced small to moderate amounts of fluorescence in preparations extracted sequentially with RNase and DNase. All of the fluorochromes could be considered "structural probes" since they produced less fluorescence in the highly condensed chromatin of thymocyte nuclei than they did in the less condensed chromatin of hepatocyte nuclei. When exposed to continuous excitation for 2-min intervals, hepatocyte nuclei stained with Nuclear Yellow or D261/37 gradually lost, respectively, approximately 21% or nearly 60% of their original fluorescence. Nuclei stained with the other three fluorochromes displayed much more rapid fading and lost more than 80% of their original fluorescence.
对五种基本荧光染料进行了评估,以确定是否有任何一种可用于微量荧光测定研究,以选择性地显示核酸。仅发现两种荧光染料——核黄(Hoechst 769121)和苯氧基吲哚化合物D261/37——对核酸具有选择性,而其他三种荧光染料在用核糖核酸酶和脱氧核糖核酸酶依次提取的制剂中产生少量至中等量的荧光。所有荧光染料都可被视为“结构探针”,因为它们在胸腺细胞核高度浓缩的染色质中产生的荧光比在肝细胞核浓缩程度较低的染色质中产生的荧光少。当以2分钟的间隔暴露于连续激发时,用核黄或D261/37染色的肝细胞核分别逐渐损失其原始荧光的约21%或近60%。用其他三种荧光染料染色的细胞核显示出更快的褪色,损失了超过80%的原始荧光。