首页> 外文期刊>Journal of Immunological Methods >Comparison of electrochemiluminescence assay and ELISA for the detection of Clostridium botulinum type B neurotoxin.
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Comparison of electrochemiluminescence assay and ELISA for the detection of Clostridium botulinum type B neurotoxin.

机译:电化学发光检测法和ELISA检测肉毒梭菌B型神经毒素的比较。

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We compared the ELISA and electrochemiluminescence (ECL) immunoassay technologies for the detection of botulinum type B neurotoxin (BotNT B), which requires highly sensitive techniques due to its potent biological activity. BotNT B complexes are the naturally secreted form of the toxin, approximately a third of which consists of the neurotoxin itself; they were aliquoted and frozen for this study. Results of both techniques were interpreted with the same standard statistical tests (ANOVA and Tukey). We first compared two commercial assays for BotNT B: the detection limit of the colorimetric ELISA was 1.56 ng/ml BotNT B complexes versus 0.39-0.78 ng/ml in the ECL test. We then used the same monoclonal antibody and the same polyclonal antibody, respectively purified by protein A and protein G chromatography, to optimize an in-house ELISA test and an in-house ECL test, making it possible to directly compare the two technologies without interference due to the properties of the antibodies used in the two tests. The colorimetric in-house ELISA had a detection threshold of 3.12 ng/ml versus the in-house ECL test whose detection threshold was 0.78-1.56 ng/ml. Thus, in both cases, the ECL assay was two to four times more sensitive than the colorimetric ELISA. The ECL assay was also more rapid (2.5 h for the in-house ECL versus 5 h for in-house ELISA with precoated wells). Overall, these elements can be used to compare the qualities of the two technologies, at least for the detection of protein antigens such as toxins.
机译:我们比较了ELISA和电化学发光(ECL)免疫测定技术检测肉毒杆菌B型神经毒素(BotNT B)的方法,由于其强大的生物活性,因此需要高度敏感的技术。 BotNT B复合物是毒素的自然分泌形式,其中约三分之一由神经毒素本身组成。将它们等分并冷冻用于本研究。两种技术的结果均使用相同的标准统计检验(ANOVA和Tukey)进行解释。我们首先比较了两种商业化的BotNT B检测方法:比色ELISA的检测限为1.56 ng / ml BotNT B复合物,而ECL测试为0.39-0.78 ng / ml。然后,我们使用分别通过蛋白A和蛋白G色谱法纯化的相同单克隆抗体和相同多克隆抗体来优化内部ELISA测试和内部ECL测试,从而可以直接比较两种技术而不会产生干扰由于两次测试中使用的抗体的特性。内部比色法ELISA的检测阈值为3.12 ng / ml,而内部ECL测试的阈值为0.78-1.56 ng / ml。因此,在这两种情况下,ECL分析的灵敏度都比色ELISA高2-4倍。 ECL测定也更快(内部ECL为2.5小时,而带有预包被孔的内部ELISA为5小时)。总体而言,这些元素可用于比较两种技术的质量,至少用于检测蛋白质抗原(如毒素)。

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