Van der Loos C M, Naruko T, Becker A E
Department of Cardiovascular Pathology, Academical Medical Center, Amsterdam, The Netherlands.
Histochem J. 1996 Oct;28(10):709-14. doi: 10.1007/BF02409008.
The newly developed peroxidase-labelled Enhanced Polymer One-Step (EPOS) reagents were applied, together with an unlabelled primary mouse antibody, in a multistep double-labelling protocol. Enzyme label reporter combinations consisted of either peroxidase and alkaline phosphatase in red and blue, respectively, or beta-galactosidase and alkaline phosphatase in turquoise and red, respectively. The latter enzyme combination was introduced using a rabbit antiperoxidase antibody and an enzyme-labelled anti-rabbit immunoglobulin antibody. The multistep procedure was tested using five different antibody combinations on cryostat and Carnoy- or formalin-fixed, paraffin-embedded sections. In each instance, clear and distinct labelling was obtained, either with the two antigens at separate sites, or with an overlap in distribution. In the latter situation, the sites of co-localization were marked by mixed colours, which were distinct and readily discriminated from the two basic colours.
新开发的过氧化物酶标记增强聚合物一步法(EPOS)试剂与未标记的小鼠一抗一起用于多步双重标记方案中。酶标记报告物组合分别由红色的过氧化物酶和蓝色的碱性磷酸酶组成,或者由蓝绿色的β-半乳糖苷酶和红色的碱性磷酸酶组成。后一种酶组合是通过兔抗过氧化物酶抗体和酶标记的抗兔免疫球蛋白抗体引入的。在低温恒温器以及用卡诺氏液或福尔马林固定、石蜡包埋的切片上,使用五种不同的抗体组合对该多步程序进行了测试。在每种情况下,无论是两种抗原位于不同部位,还是分布有重叠,都能获得清晰、明显的标记。在后一种情况下,共定位位点由混合颜色标记,这些混合颜色明显且易于与两种基本颜色区分开来。