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商业多克隆和单克隆组织染色PAP试剂盒。免疫过氧化物酶试剂及其与自制免疫试剂相比的性能特征。

Commercial polyclonal and monoclonal histostaining PAP kits. Immunoperoxidase reagents and performance characteristics in comparison with self-prepared immunoreagents.

作者信息

Kuhlmann W D, Peschke P

出版信息

Histochemistry. 1985;82(5):411-9. doi: 10.1007/BF02450474.

Abstract

Universal, polyclonal and monoclonal immunoperoxidase staining kits from BioGenex, Dako and Ortho were employed for the localization of antigens such as gastrin, prostate specific antigen, IgA, IgG, AFP and CEA in histological sections from formaldehyde fixed and paraffin embedded human specimens. The kit components were controlled by immunohistological and serological assays and were also compared with self-prepared reagents. In connection with specific primary antibodies, universal/basic kits gave reliable localization of defined antigens. The optimal concentration of the primary antibodies had to be established by dilution experiments. In the case of polyclonal kits, typical antigen localization was obtained in selected tissue sections with all the respective kits. CEA kits also stained strongly NCA molecules present in organs such as colon, stomach and liver. BioGenex polyclonal kits gave almost stronger stainings than kits from Dako and Ortho. Irrespective of which kit from different commercial sources is used, development of peroxidase activity with AEC/H2O2 often had to be stopped far below the recommended incubation time of 40 min or overstaining with color change from reddish to muddy green occurred. The latter was attributed to insufficiently balanced kit reagents, an interpretation which was supported by quantitative serological studies. Sensitivity of immunohistological reactivity was much enhanced by pretreatment of tissue sections with Pronase. Thus, stronger immunostainings and larger numbers of positive cells were detected than in conventionally rehydrated sections.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

使用来自BioGenex、Dako和Ortho的通用、多克隆和单克隆免疫过氧化物酶染色试剂盒,对甲醛固定、石蜡包埋的人体标本组织切片中的胃泌素、前列腺特异性抗原、IgA、IgG、甲胎蛋白和癌胚抗原等抗原进行定位。试剂盒组件通过免疫组织学和血清学检测进行控制,并与自制试剂进行比较。与特定的一抗结合,通用/基础试剂盒能可靠地定位特定抗原。一抗的最佳浓度必须通过稀释实验来确定。对于多克隆试剂盒,在选定的组织切片中使用所有相应试剂盒均获得了典型的抗原定位。癌胚抗原试剂盒也能强烈染色存在于结肠、胃和肝脏等器官中的NCA分子。BioGenex多克隆试剂盒的染色效果几乎比Dako和Ortho的试剂盒更强。无论使用不同商业来源的哪种试剂盒,用AEC/H2O2进行过氧化物酶活性显色时,往往不得不在远低于推荐的40分钟孵育时间时就停止,否则会出现过度染色,颜色从微红变为泥绿色。后者归因于试剂盒试剂平衡不足,这一解释得到了定量血清学研究的支持。用链霉蛋白酶预处理组织切片可大大提高免疫组织学反应的敏感性。因此,与传统复水切片相比,检测到更强的免疫染色和更多的阳性细胞。(摘要截短于250字)

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