Blest A D, Davie P S
Stain Technol. 1977 Sep;52(5):273-5. doi: 10.3109/10520297709116793.
Arthropod central nervous tissue is fixed for 1 hr at 20 C in 8% pure formic acid in 1:1 n-butanol/n-propanol prepared immediately before use (FBP), then washed for 15-30 min in 90% ethanol, and embedded in paraffin wax. Impregnation is by modified Ungewitter techniques in which the silver bath is preceded by mercury/cobalt mordanting, or by modified Holmes' methods following similar mordanting procedures. The methods yield high resolution of axons with minimal background staining, while the staining of neuronal somata is suppressed. They succeed with brains of crustacea and Odonata and other difficult materials. Tissues fixed in FBP are hard and require care in sectioning.
节肢动物中枢神经组织在20℃下用临用前配制的1:1正丁醇/正丙醇中的8%纯甲酸固定1小时(FBP),然后在90%乙醇中洗涤15 - 30分钟,再嵌入石蜡。浸染采用改良的Ungewitter技术,在银浴之前进行汞/钴媒染,或采用类似媒染程序后用改良的Holmes方法。这些方法能以最小的背景染色获得高分辨率的轴突,同时抑制神经元胞体的染色。它们适用于甲壳类动物和蜻蜓目昆虫的大脑以及其他难处理的材料。用FBP固定的组织很硬,切片时需要小心。