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利用转移模板溶血斑点试验筛选和复制抗半抗原杂交瘤

Screening and replica plating of anti-hapten hybridomas with a transfer template hemolytic spot assay.

作者信息

Bankert R B, DesSoye D, Powers L

出版信息

J Immunol Methods. 1980;35(1-2):23-32. doi: 10.1016/0022-1759(80)90147-7.

Abstract

A localized hemolysis in gel assay is described for screening microcultures of hybridomas for the production of anti-hapten antibody. The keys to the rapid screening assay reported here are a special fenestrated transfer template and an improved hapten conjugated target cell. The transfer template is a 96-well plate with a calibrated hole in the bottom center of each well. To assay for anti-hapten antibodies, the transfer template is positioned over a 96-well microculture plate containing the growing hybridomas. After making contact with the tissue culture supernatant each orifice of the transfer template retains approximately 2 microliter of tissue culture supernatant. The transfer template is then placed onto an assay slide containing a thin layer of hapten conjugated target erythrocytes incorporated into agarose. After incubation with an anti-immunoglobulin and complement, areas of localized hemolysis in the gel indicate hybridomas which are secreting anti-hapten antibodies. The assay detects as little as 10 pg of antibody. Since the transfer template can be used as a replica plate, one can repeatedly transfer samples to various slides which contain either different hapten target cells or different hapten analog inhibitors in the agarose layer. Therefore, in addition to rapidly screening microcultures for positive hybridomas this procedure permits the characterization of each monoclonal antibody's fine specificity.

摘要

本文描述了一种用于筛选杂交瘤微培养物中抗半抗原抗体产生的凝胶分析中的局部溶血方法。这里报道的快速筛选分析的关键是一种特殊的有孔转移模板和一种改进的半抗原偶联靶细胞。转移模板是一个96孔板,每个孔底部中心有一个校准孔。为了检测抗半抗原抗体,将转移模板放置在含有正在生长的杂交瘤的96孔微培养板上。转移模板的每个孔与组织培养上清液接触后,会保留约2微升的组织培养上清液。然后将转移模板放置在一个检测载玻片上,该载玻片含有一层掺入琼脂糖中的半抗原偶联靶红细胞薄层。在用抗免疫球蛋白和补体孵育后,凝胶中局部溶血的区域表明杂交瘤正在分泌抗半抗原抗体。该分析可检测低至10 pg的抗体。由于转移模板可用作复制板,因此可以将样品重复转移到各种载玻片上,这些载玻片在琼脂糖层中含有不同的半抗原靶细胞或不同的半抗原类似物抑制剂。因此,除了快速筛选微培养物中的阳性杂交瘤外,该方法还可以表征每种单克隆抗体的精细特异性。

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