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A silver impregnation method for neurons in the central nervous system of the small laboratory animals.

作者信息

Ogawa Y

机构信息

Department of Anatomy, Nihon University School of Medicine, Tokyo, Japan.

出版信息

Okajimas Folia Anat Jpn. 1992 May;69(1):75-6. doi: 10.2535/ofaj1936.69.1_75.

Abstract

Brains of small, adult laboratory animals, fixed by formalin-perfusion, and cut into pieces usually 2-3 mm thick X 3-5 mm2 are placed into a solution containing: 7% aqueous solution of potassium dichromate 100 ml, 99.5% ethyl alcohol 40 ml, concentrated formalin 10 ml, distilled water 50 ml, for 24 hours. The process is repeated with a freshly prepared solution for another 24 hours. The pieces are then transferred to a 3.5% aqueous solution of potassium dichromate for 48 hours, and then to a 1% aqueous solution of silver nitrate for 48 hours. Frozen or celloidin sections 70-100 microns in thickness are put into 90% and then into 100% ethyl alcohol for 30 minutes respectively, creosote-benzene (1:1), benzene and mounted with or without cover glass applying Entellan neu. This procedure gives high quality impregnation and it takes about one week to complete.

摘要

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