Paterson Jennifer C, Ballabio Erica, Mattsson Göran, Turner Susan H, Mason David Y, Marafioti Teresa
Leukaemia Research Immunodiagnostics Unit, Nuffield Department of Clinical Laboratory Sciences, University of Oxford, Oxford, UK.
Appl Immunohistochem Mol Morphol. 2008 Jul;16(4):371-81. doi: 10.1097/PAI.0b013e318164fc63.
Double immunoenzymatic labeling of 2 different molecules in tissue sections is a widely used technique. However, it is time consuming since the 2 immunoenzymatic procedures are carried out in sequence, and they must also be optimally performed to avoid unwanted background labeling. In this paper, we report that double immunoenzymatic staining performed using automated immunostaining apparatus considerably reduces the requirements in terms of time and is also highly reproducible and free of background. Three tissue markers can also be visualized by performing (after immunoperoxidase labeling) 2 sequential immuno-alkaline phosphatase procedures using different substrates. Furthermore, single or double detection of mRNA by in situ hybridization can be combined with immunoenzymatic labeling. Finally, automated labeling could also be performed on peripheral blood and bone marrow smears, opening the possibility of using this procedure in the analysis of hematologic/cytology samples.
在组织切片中对两种不同分子进行双重免疫酶标记是一种广泛应用的技术。然而,由于两种免疫酶程序是按顺序进行的,所以该技术耗时较长,而且还必须优化操作以避免出现不必要的背景标记。在本文中,我们报告称,使用自动免疫染色设备进行双重免疫酶染色可大幅减少时间需求,而且具有高度的可重复性且无背景。通过(免疫过氧化物酶标记后)使用不同底物进行两步连续免疫碱性磷酸酶程序,还可使三种组织标志物可视化。此外,原位杂交对mRNA的单重或双重检测可与免疫酶标记相结合。最后,自动标记也可在外周血和骨髓涂片上进行,从而为在血液学/细胞学样本分析中使用该程序开辟了可能性。