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Chromogen-based Immunohistochemical Method for Elucidation of theCoexpression of Two Antigens Using Antibodies from the Same Species

机译:基于色原的免疫组织化学方法阐明使用相同物种的抗体共表达两种抗原

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摘要

The authors established a chromogen-based, double immunolabeling method using antibodies from the same species without any unwanted cross-reactivity. In addition, time-consuming staining steps were shortened by using polymer-based secondary antibodies. Taking advantage of the nature of the chromogen 3-amino-9-ethylcarbazole (AEC), which is used as a horseradish peroxidase substrate for antibody detection, the AEC-derived signals in the first color development were easily eliminated by alcohol treatment. Therefore, the signals from the first staining did not interfere with those from the subsequent second staining, which used the chromogen 3,3′-diaminobenzidine. The co-localization of antigens within the same cell could be confirmed using this method, because cell images of the individual dye staining steps could be obtained and developed. The images from each step could be expressed in pseudo-colors in a dark field by using a computer. As a result, merged images could be constructed that resembled the images acquired by the fluorescent immunolabeling technique. The resolution of this method enabled analysis of the coexpression of two antigens in the same cell in the same section. The authors have named this staining technique the elucidation of the coexpression of two antigens in a cell using antibodies from the same species (ECSS).
机译:作者建立了一种基于色原的双重免疫标记方法,该方法使用了来自相同物种的抗体,而没有任何不需要的交叉反应性。另外,通过使用基于聚合物的二抗缩短了费时的染色步骤。利用发色团3-氨基-9-乙基咔唑(AEC)的性质(用作辣根过氧化物酶底物进行抗体检测),可以通过酒精处理轻松消除第一次显色中AEC衍生的信号。因此,第一次染色的信号不会干扰随后的第二次染色的信号,后者使用了显色剂3,3'-二氨基联苯胺。使用此方法可以确认抗原在同一细胞内的共定位,因为可以获取并显影各个染料染色步骤的细胞图像。来自每个步骤的图像可以使用计算机在暗场中以伪彩色表示。结果,可以构建与通过荧光免疫标记技术获得的图像相似的合并图像。此方法的分辨率可分析同一部分中同一细胞中两种抗原的共表达。作者已将此染色技术命名为使用同一物种的抗体(ECSS)阐明细胞中两种抗原共表达的方法。

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