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A microwave antigen retrieval method using two heating steps for enhanced immunostaining on aldehyde-fixed paraffin-embedded tissue sections

机译:一种微波抗原回收方法,采用两个加热步骤,可增强醛固定石蜡包埋的组织切片的免疫染色

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摘要

Antigen retrieval is an immunohistochemical procedure that results in better exposure of target antigens in aldehyde-fixed, paraffin-embedded tissue sections to antibodies. However, the commercially recommended or conventional protocols for antigen retrieval do not always succeed in expressing the target antigen. Here, an improved method was developed for antigen retrieval from aldehyde-fixed, paraffin-embedded histological sections. Proliferating cell nuclear antigen (PCNA), tight junction proteins Claudin-2 and Claudin-7, and water channel aquaporins in kidney tissue were selected as test antigens. Typically, PCNA and Claudin-2 and Claudin-7 show negative, weak, or nonspecific immunoreactions with conventional antigen retrieval methods using microwave heating. In the present study, microwave heating was performed twice with an interval of 30 min between the two steps to allow the buffer solution to cool. Sodium citrate buffer (10 mM sodium citrate, pH 6.0) was used for PCNA, and Tris-EDTA buffer (10 mM Tris, 1 mM EDTA, pH 9.0) was used for the Claudins. Compared with conventionally prepared tissues, the tissues exhibited both enhanced and specific immunostaining, and well-preserved morphology. In conclusion, the conventional protocol could be supplemented with a second microwave heating step to improve the expression of antigens that do not respond well to the conventional method.
机译:抗原修复是一种免疫组织化学程序,可将醛固定,石蜡包埋的组织切片中的目标抗原更好地暴露于抗体。然而,商业上推荐的或常规的用于抗原回收的方案并不总是成功地表达靶抗原。在这里,开发了一种改进的方法,用于从醛固定,石蜡包埋的组织学切片中回收抗原。选择肾组织中的增殖细胞核抗原(PCNA),紧密连接蛋白Claudin-2和Claudin-7以及水通道水通道蛋白作为测试抗原。通常,PCNA和Claudin-2和Claudin-7在使用微波加热的常规抗原回收方法中显示出阴性,弱或非特异性免疫反应。在本研究中,微波加热进行两次,两次之间间隔30分钟,以使缓冲液冷却。 PCNA使用柠檬酸钠缓冲液(10 mM柠檬酸钠,pH 6.0),Claudins使用Tris-EDTA缓冲液(10 mM Tris,1 mM EDTA,pH 9.0)。与常规制备的组织相比,该组织表现出增强的和特异性的免疫染色,以及保存良好的形态。总而言之,可以在常规方案中增加第二个微波加热步骤,以改善对常规方法反应不佳的抗原的表达。

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