Szegedi Z, Amin F, Szende B, Bowen I D
Joint Research Organization of the Hungarian Academy of Sciences and Semmelweis University of Medicine, 1st Institute of Pathology and Experimental Cancer Research, Department of Molecular Pathology, Budapest, Hungary.
Pathol Oncol Res. 1998;4(3):217-23. doi: 10.1007/BF02905252.
The aim of the study was to work out a technique for the detection of acid phosphatase enzyme activity by confocal laser-scanning microscope using the histochemical acid phosphatase detection method (after Barka and Anderson 1962, modified by Bowen and Lewis 1985) routinely used for light microscopy. The density and the distribution of enzyme reaction product is dependent on the incubation time, as shown by different confocal images or ELISA reader. The inhibition of the enzyme activity with metal ions shows the same profile known from the literature. This staining method seems to be useful to demonstrate subcellular distribution of the enzyme in the lysosomes and in the Golgi apparatus.
本研究的目的是开发一种技术,通过共聚焦激光扫描显微镜,利用常规用于光学显微镜的组织化学酸性磷酸酶检测方法(基于1962年巴尔卡和安德森的方法,1985年由鲍温和刘易斯修改)来检测酸性磷酸酶的酶活性。如不同的共聚焦图像或酶标仪所示,酶反应产物的密度和分布取决于孵育时间。金属离子对酶活性的抑制呈现出文献中已知的相同模式。这种染色方法似乎有助于显示该酶在溶酶体和高尔基体中的亚细胞分布。