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一种用于制备用于光学显微镜和电子显微镜观察的组织培养克隆的快速方法。

A rapid method for preparing tissue culture clones for light and electron microscopy.

作者信息

Lindsey J N, Brackeen R B, Steinberger A

出版信息

Tex Rep Biol Med. 1975;33(4):519-23.

PMID:59955
Abstract

Fixation and epoxy-embedment of tissue culture clones in situ were carried out in Falcon tissue culture plates. The clone of cells, retained at one end of the casting, was stained with azure II-methylene blue and then studied with the oil immersion objective. The dimensions of the epoxy casting were ideal for mouting as a block in conventional ultramicrotone chucks. The use of one epoxy casting permits a single preparation of tissue culture clones for direct light microscopic observations and subsequently for ultramicrotomy.

摘要

在Falcon组织培养板中对组织培养克隆进行原位固定和环氧树脂包埋。保留在铸型一端的细胞克隆用天青II-亚甲蓝染色,然后用油浸物镜进行观察。环氧树脂铸型的尺寸非常适合作为一个块安装在传统超薄切片机夹头中。使用一个环氧树脂铸型可对组织培养克隆进行单次制备,用于直接光学显微镜观察,随后用于超薄切片术。

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