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Highly sensitive detection of target molecules using a new fluorescence-based bead assay

机译:使用新的基于荧光的珠子测定的靶分子的高度敏感性检测

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Development of immunoassays with improved sensitivity, specificity and reliability are of major interest in modern bioanalytical research. We describe the development of a new immunomagnetic fluorescence detection (IM-FD) assay based on specific antigen/antibody interactions and on accumulation of the fluorescence signal on superparamagnetic PE beads in combination with the use of extrinsic fluorescent labels. IM-FD can be easily modified by varying the order of coatings and assay conditions. Depending on the target molecule, antibodies (ABs), entire proteins, or small protein epitopes can be used as capture molecules. The presence of target molecules is detected by fluorescence microscopy using fluorescently labeled secondary or detection antibodies. Here, we demonstrate the potential of the new assay detecting the two tumor markers IGF-I and p53 antibodies in the clinically relevant concentration range. Our data show that the fluorescence-based bead assay exhibits a large dynamic range and a high sensitivity down to the subpicomolar level.
机译:具有改善的敏感性,特异性和可靠性的免疫测定的发展是对现代生物分析研究的主要兴趣。我们描述了基于特异性抗原/抗体相互作用的新免疫磁性荧光检测(IM-FD)测定和荧光信号与外在荧光标记的结合结合的荧光信号的发展。通过改变涂层和测定条件的顺序,可以容易地修改IM-FD。取决于靶分子,抗体(ABS),整个蛋白质或小蛋白质表位可以用作捕获分子。使用荧光标记的二次或检测抗体通过荧光显微镜检测靶分子的存在。在这里,我们证明了在临床相关浓度范围内检测到两个肿瘤标志物IGF-1和P53抗体的新测定的潜力。我们的数据表明,荧光的珠子测定表现出大的动态范围和低敏感性下降至亚磷莫马尔水平。

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