Using Antibodies in Microscopy: A Guide to Immunohistochemistry. Part 2: IHC Staining Protocols

C. Guerin
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引用次数: 1

Abstract

Immunohistochemistry (IHC) is the use of antibodies as probes to determine the localization of proteins in a cell or tissue sample. In microscopy, the technique has been in use since the 1940s by pathologists and research scientists. At first glance it appears a straightforward procedure. However, in practice, an IHC protocol has a number of steps where problems can occur, resulting in either false positive or false negative data. IHC can be used in both transmitted light and fluorescence microscopy, and it can be used in combinations to identify and mark multiple proteins of interest. While the technique has been published extensively, a certain amount of confusion exists as to how to optimize it. This series of three articles describes the steps involved in IHC, their function, and some variations that occur in specific protocols on differing cell and tissue types. It is hoped that a better understanding of these steps will help to guide users in determining the optimal conditions for carrying through IHC protocols.
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在显微镜下使用抗体:免疫组织化学指南。第2部分:IHC染色协议
免疫组织化学(IHC)是使用抗体作为探针来确定细胞或组织样本中蛋白质的定位。在显微镜方面,这项技术自20世纪40年代以来一直被病理学家和研究科学家使用。乍一看,这似乎是一个简单的过程。然而,在实践中,IHC协议有许多步骤可能会出现问题,从而导致假阳性或假阴性数据。IHC既可用于透射光显微镜,也可用于荧光显微镜,还可组合用于识别和标记多种感兴趣的蛋白质。虽然这项技术已经广泛发表,但对于如何优化它仍存在一定的困惑。这一系列的三篇文章描述了IHC涉及的步骤、它们的功能,以及在不同细胞和组织类型的特定方案中发生的一些变化。希望更好地了解这些步骤将有助于指导用户确定执行IHC协议的最佳条件。
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