Newman G R, Jasani B
Medical Microscopy Sciences, Department of Pathology, University of Wales College of Medicine, Heath Park, Cardiff, UK.
Histochem J. 1998 Sep;30(9):635-45. doi: 10.1023/a:1003404128497.
Potentially, silver development could unify most modern demands for clean, accurately localized marker amplification in microscopy and bioanalysis. However, the existing technology leaves room for improvement in developer design. A new formulation has been devised which, by using principles of silver chelation, avoids problems of self-nucleation and catalysis by light. It is made, just before use, by mixing together equal amounts of stock solutions containing high molarity, Tris-buffered silver nitrate and alcoholic, buffered pyrogallol. The two stocks are easily prepared and have very long shelf-lives. The developer is light insensitive for up to an hour at room temperature, so that development can proceed under ambient light conditions and at the neutral pH most suited to biological systems. The powerful reducer in the suggested formulation should allow the detection of low concentrations of marker signal in a wide range of applications.
从潜在意义上讲,银显影技术有望满足现代显微镜学和生物分析中对清洁、精确定位的标记物扩增的大多数需求。然而,现有技术在显影剂设计方面仍有改进空间。一种新配方已经设计出来,通过运用银螯合原理,避免了自核化和光催化问题。它在使用前通过将等体积的高摩尔浓度、三羟甲基氨基甲烷缓冲硝酸银储备溶液和酒精缓冲邻苯三酚储备溶液混合制成。这两种储备溶液易于制备且保质期很长。该显影剂在室温下长达一小时对光不敏感,因此显影可以在环境光条件下以及最适合生物系统的中性pH值下进行。建议配方中的强力还原剂应能在广泛的应用中检测到低浓度的标记信号。