首页> 外文期刊>Analytical and bioanalytical chemistry >Fluorescence-labelled antigen-binding fragments (Fab) from monoclonal antibody 5F12 detect human erythropoietin in immunoaffinity capillary electrophoresis
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Fluorescence-labelled antigen-binding fragments (Fab) from monoclonal antibody 5F12 detect human erythropoietin in immunoaffinity capillary electrophoresis

机译:单克隆抗体5F12的荧光标记抗原结合片段(Fab)在免疫亲和毛细管电泳中检测人促红细胞生成素

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摘要

A faster and more convenient method is required for the detection of recombinant erythropoietin (Epo) in human body fluids. In the present study we wanted to elucidate the principal suitability of immunoaffinity capillary electrophoresis (CE) in this respect. CE offers itself as a high-speed, high-throughput technique provided a suitable affinity reagent is available. We chose monoclonal antibody 5F12 from Amgen which binds to a conformation-independent epitope in the N-terminal region of the human Epo protein. For CE with laser-induced fluorescence detection it was necessary to produce fluorescently labelled antibody with one single antigen binding site. Monomeric antigen-binding fragments (Fab) were obtained by site-selective cleavage of the pure antibody and labelled with the fluorescent dye, Alexa Fluor 488. The mixture of labelled isomers was partially resolved by ion exchange HPLC and isoelectric focusing. The fluorescent Fab could be used to detect erythropoietin by immunoaffinity capillary isoelectric focusing and zone capillary electrophoresis via its antigen complex.
机译:需要一种更快,更方便的方法来检测人体液中的重组促红细胞生成素(Epo)。在本研究中,我们想阐明免疫亲和毛细管电泳(CE)在这方面的主要适用性。只要有合适的亲和试剂,CE就会提供自己的高速,高通量技术。我们从Amgen选择单克隆抗体5F12,该抗体与人Epo蛋白N端区域的构象非依赖性表位结合。对于具有激光诱导的荧光检测的CE,必须产生具有一个单一抗原结合位点的荧光标记抗体。单体抗原结合片段(Fab)通过纯抗体的定点切割获得,并用荧光染料Alexa Fluor 488标记。通过离子交换HPLC和等电聚焦,部分分离了标记异构体的混合物。荧光Fab可用于通过免疫亲和毛细管等电聚焦和通过其抗原复合物的区域毛细管电泳检测促红细胞生成素。

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