Martin J H, Marcus P B
Ultrastruct Pathol. 1983 Mar-Apr;4(2-3):261-4. doi: 10.3109/01913128309140795.
The need to examine certain components of a specimen with the electron microscope is frequently recognized only after study of the paraffin sections, by which time the total specimen has usually been fixed in Formalin. Such specimens are frequently large, with the result that representative samples for electron microscopy may be difficult to isolate. A simple, quick, and inexpensive method for overcoming this sampling problem is described. This technique is best employed in laboratories that routinely use a single tissue fixative suitable for both light and electron microscopy. The specimen is taken direct from the Formalin, and very thin slices are prepared by hand with a blade, stained with methylene blue, and examined in the wet state under the microscope. On identification, representative tissue is removed by micro-dissection and processed further for electron microscopy.
通常只有在对石蜡切片进行研究之后,才会认识到需要用电子显微镜检查标本的某些成分,而此时整个标本通常已用福尔马林固定。这类标本通常很大,结果可能难以分离出用于电子显微镜检查的代表性样本。本文描述了一种简单、快速且廉价的方法来克服这一取样问题。该技术最适合在常规使用适用于光学显微镜和电子显微镜的单一组织固定剂的实验室中使用。标本直接从福尔马林中取出,用刀片手工制备非常薄的切片,用亚甲蓝染色,并在湿态下于显微镜下检查。识别后,通过显微解剖取出代表性组织,并进一步处理用于电子显微镜检查。