Bedi K S, Horobin R W
Histochemistry. 1976 Aug 12;48(2):153-9. doi: 10.1007/BF00494553.
A schedule for staining partially hydrated PAS-positive structures using non-aqueous solutions has been devised. Tissues are dewaxed, taken down to 70% alcohol, oxidised for 10 min in a 1% w/v alcoholic solution of periodic acid, treated with an alcoholic solution of phosphotungstic acid-Schiff reagent complex (PTA-Schiff reagent) for 25 min, washed in alcohol, cleared in xylene and mounted in a synthetic medium. The PTA-Schiff reagent complex prepared from de Tomasi Schiff reagent by precipitation with PTA may be stored in the deep freeze for many months and dissolved freshly in alcohol for use. The PTA-Schiff reagent used as above allows staining of highly water soluble materials such as dextran. From blocking and digestion studies the mode of action seems similar to de Tomasi Schiff reagent. The partial hydration of the tissues prior to reaction was found to be essential for effective staining.
已设计出一种使用非水溶液对部分水合的PAS阳性结构进行染色的方案。组织进行脱蜡处理,降至70%酒精浓度,在1%(重量/体积)的高碘酸酒精溶液中氧化10分钟,用磷钨酸-席夫试剂复合物(PTA-席夫试剂)的酒精溶液处理25分钟,用酒精洗涤,用二甲苯透明,然后封固在合成介质中。由德托马西席夫试剂通过与PTA沉淀制备的PTA-席夫试剂复合物可在深冻条件下储存数月,使用时新鲜溶解于酒精中。上述使用的PTA-席夫试剂可对高度水溶性物质如右旋糖酐进行染色。从封闭和消化研究来看,其作用方式似乎与德托马西席夫试剂相似。发现反应前组织的部分水合对于有效染色至关重要。