微波加热在福尔马林固定组织切片中提取抗原对广泛抗体的影响。

Histochemistry Pub Date : 1994-09-01 DOI:10.1007/BF00268892
R von Wasielewski, M Werner, M Nolte, L Wilkens, A Georgii
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引用次数: 56

摘要

常规目的活检标本的甲醛固定经常被认为是免疫组织化学研究重复性差的原因。近年来,利用微波辐射进行抗原回收(AGR)被认为是一种有潜力的增强免疫染色的工具。将52个标记物分别用甲醛固定24 h、1 ~ 6周和3年的组织及咨询病例材料进行常规染色和微波加热后染色的比较。在足够的固定时间(24小时)后,只有少数标记物(17%)在AGR后表现出更好的结果,但当组织固定时间较长时,这一比例增加到50%。在固定时间和组织处理时间未知的会诊病例组中获得了最大的增强(58%的测试标记物显示出更好的染色结果)。为了获得可靠的AGR增强,持续加热(100℃)不应短于20分钟。总之,如果严格评估,AGR可能成为简化和均衡免疫组织化学技术的最重要工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of antigen retrieval by microwave heating in formalin-fixed tissue sections on a broad panel of antibodies.

Formaldehyde fixation of biopsy specimens for routine purposes has often been held responsible for the poor reproducibility of immunohistochemical studies. Recently, antigen retrieval (AGR) using microwave irradiation was described as a potential tool to enhance immunostaining. A comparison of conventional staining and staining after microwave heating was performed for 52 markers, using tissues fixed in formaldehyde for 24 h, 1 to 6 weeks and 3 years respectively, as well as consultant case material. After adequate duration of fixation (24 h), only a few markers (17%) showed better results after AGR, but this percentage was increased to 50% when tissues were fixed for longer periods. Maximal enhancement was obtained in the group of consultant cases (58% of tested markers demonstrated better staining results), in which the period of fixation and tissue processing was unknown. To achieve reliable enhancement with AGR, continuous heating (100 degrees C) should not be shorter than 20 min. In conclusion, AGR may become the most important tool to simplify and equalize immunohistochemical techniques, if critically evaluated.

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