Ren Ke, Dai Yidan, Yi Kai, Kinoshita Masanobu, Itoh Masahiro, Sakata Ichiro, Sakai Takafumi, Yi Shuang-Qin
Department of Frontier Health Sciences, Graduate School of Human Health Sciences, Tokyo Metropolitan University.
Department of Anatomy, Tokyo Medical University.
J Vis Exp. 2017 Jun 15(124):55483. doi: 10.3791/55483.
This work describes the whole-mount immunohistochemistry staining method in detail, using neurofilament protein antibody to label the innervation of the biliary tract in Suncus murinus (S. murinus ). First, the specimen was dissected from S. murinus and fixed in 4% paraformaldehyde (PFA). Second, an enzymatic treatment and potential endogenous peroxidase inactivation were performed. The specimen was then exposed to the primary antibody, anti-neurofilament protein antibody, for 3-6 days. It was then incubated with the secondary antibody conjugated with horseradish peroxidase. The color reaction was revealed by reacting the specimen with a 3,3'-diaminobenzidine (DAB) substrate. This method can be applied to analyze the innervation of all visceral organs. Furthermore, this protocol can also be adapted to test other neuronal antibodies, but optimization of the antibodies should be done first. This method was originally introduced by Kuratani and Tanaka.
这项工作详细描述了全组织免疫组化染色方法,使用神经丝蛋白抗体标记家鼩(Suncus murinus)胆道的神经支配。首先,从家鼩身上解剖出标本并固定于4%多聚甲醛(PFA)中。其次,进行酶处理和潜在内源性过氧化物酶灭活。然后将标本与一抗,即抗神经丝蛋白抗体,孵育3 - 6天。接着用与辣根过氧化物酶偶联的二抗进行孵育。通过将标本与3,3'-二氨基联苯胺(DAB)底物反应来显示颜色反应。该方法可用于分析所有内脏器官的神经支配。此外,此方案也可适用于检测其他神经元抗体,但应首先对抗体进行优化。该方法最初由仓谷和田中引入。