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[使用pH值为8.0的甲醛作为电子显微镜和荧光显微镜的固定剂]

[Use of formaldehyde with pH 8 0 as a fixative for electron and fluorescence microscopy].

作者信息

Semenova L A

出版信息

Arkh Patol. 1976;38(9):61-3.

PMID:17377
Abstract

For fixation of the material to be investigated at the light and ultrastuctural level the author suggests to use 4% formaldehyde obtained by depolymerization of paraform on 0.1 M phosphate buffer with end pH 8.0 of the solution. This fixative stabilizes well glycogen and tissue structure. The ultrastructural characteristics of cells following continuous (up to 130 days) fixation are comparable with those obtained after fixation with aldehydes by conventional techniques. Results of histological PAS test, Feulgen's reactions and those to acid polycaccharides were identical to the results obtained in fixation with neutralized formalin. The possibility of prolonged storage of tissues makes it possible to perform delayed and repeated ultrastructural investigations of clinical and experimental material.

摘要

为了在光学和超微结构水平上固定待研究的材料,作者建议使用通过在0.1M磷酸盐缓冲液中解聚多聚甲醛获得的4%甲醛,溶液最终pH值为8.0。这种固定剂能很好地稳定糖原和组织结构。连续(长达130天)固定后细胞的超微结构特征与通过传统技术用醛类固定后获得的特征相当。组织学PAS试验、福尔根反应以及对酸性多糖的反应结果与用中和福尔马林固定后获得的结果相同。组织长时间保存的可能性使得对临床和实验材料进行延迟和重复的超微结构研究成为可能。

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