Rubin N H, Baur P S
Stain Technol. 1983 May;58(3):157-60. doi: 10.3109/10520298309066777.
A technique is described which facilitates histological preparation of multiple tissue specimens for light microscopy. The procedure enables the investigator to separate and label identifiable subgroups from a larger number of specimens in one histological section. After standard fixation, murine esophagi were arranged longitudinally and secured within segments of murine intestine. Markers such as plant fibers and human hairs were threaded alongside the esophagi within each intestinal casing. After standard dehydration and infiltration, several segments of intestine were arranged parallel to each other and at right angles to the intended plane of sectioning and were embedded together in one paraffin block. This method made it possible to assemble onto one microscope slide cross sections of 42 individual esophagi in 6 identifiable subgroups, each containing 7 esophagi.
本文描述了一种有助于制备用于光学显微镜检查的多个组织标本的组织学技术。该程序使研究人员能够在一个组织学切片中从大量标本中分离并标记出可识别的亚组。经过标准固定后,将小鼠食管纵向排列并固定在小鼠肠段内。诸如植物纤维和人类毛发等标记物沿着每个肠管内的食管穿线。经过标准脱水和浸润后,将几段肠管彼此平行且与预期切片平面成直角排列,并一起包埋在一个石蜡块中。这种方法使得在一张显微镜载玻片上能够组装42个单独食管的横截面,分为6个可识别的亚组,每个亚组包含7个食管。