Sato Y, Mukai K, Watanabe S, Goto M, Shimosato Y
Am J Pathol. 1986 Dec;125(3):431-5.
A new simplified tissue processing method for immunostaining was devised. Tissues were fixed in acetone at -20 C overnight, then cleared in methyl benzoate and xylene, consecutively, and embedded in ordinary paraffin at 58-60 C. Thin paraffin sections were deparaffinized with xylene, immersed in acetone and then phosphate buffered saline, and immunostained with various monoclonal and conventional antibodies, which have only been used on fresh-frozen or PLP-fixed frozen sections. As with PLP-fixed frozen sections, the following antigens were clearly demonstrated in the tissue sections processed with the present method: T (Leu-1, Leu-2a, Leu-3a, Leu-4, OKT3, OKT4, OKT8), B (B1, B2, Leu-14, IgM, IgD) lymphocyte surface markers and other antigens (Leu-7, OKT6, OKT9, OKM1, OKI1, J5, Ki-1, Ki-67, TdT, oncogene Ha-ras P21). Sections prepared by the present method demonstrated much better histologic and cytologic preservation than possible in frozen sections.
设计了一种用于免疫染色的简化组织处理新方法。将组织在-20℃的丙酮中固定过夜,然后依次用苯甲酸甲酯和二甲苯透明,并在58-60℃下嵌入普通石蜡。薄石蜡切片用二甲苯脱蜡,浸入丙酮,然后浸入磷酸盐缓冲盐水中,并用各种单克隆抗体和传统抗体进行免疫染色,这些抗体以前仅用于新鲜冷冻或PLP固定的冰冻切片。与PLP固定的冰冻切片一样,用本方法处理的组织切片中可清楚显示下列抗原:T(Leu-1、Leu-2a、Leu-3a、Leu-4、OKT3、OKT4、OKT8)、B(B1、B2、Leu-14、IgM、IgD)淋巴细胞表面标志物及其他抗原(Leu-7、OKT6、OKT9、OKM1、OKI1、J5、Ki-1、Ki-67、TdT、癌基因Ha-ras P21)。用本方法制备的切片在组织学和细胞学保存方面比冰冻切片更好。