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Antigen capture anti-dengue IgA ELISA for the detection of flavivirus specific antibodies (ACA-ELISA)

机译:抗原捕获抗登革热IgA ELISA用于检测黄病毒特异性抗体(ACA-ELISA)

摘要

We have developed antigen capture IgA Enzyme Immunoassay for the detection of anti-flavivirus IgA and (ACA-ELISA). The assay, flavivirus dissolved antigen, preferably using a dengue virus lysis antigen captured by the monoclonal antibody. Anti flavivirus IgA captured from the test serum is detected preferably a reporter group, for example using labeled rabbit anti-IgA horseradish peroxidase (HRP). The assay has been found to be at least 8 times more sensitive than the anti-human IgA capture ELISA (AAC-ELISA). ACA-ELISA based on either serum or saliva, it has been found to be a rapid at higher sensitivity compared with the "Golden Rule" anti-dengue IgM detection techniques. This can be used as a diagnostic tool for dengue confirmation in early infection.
机译:我们已经开发了用于捕获抗黄病毒IgA和(ACA-ELISA)的抗原捕获IgA酶免疫法。该测定法是黄病毒溶解的抗原,优选使用单克隆抗体捕获的登革热病毒溶解抗原。优选地,例如使用标记的兔抗IgA辣根过氧化物酶(HRP)检测从报告血清中捕获的抗黄病毒IgA作为报道基团。已发现该测定的灵敏度比抗人IgA捕获ELISA(AAC-ELISA)高至少8倍。基于“血清或唾液”的ACA-ELISA,与“黄金法则”抗登革热IgM检测技术相比,发现具有较高的灵敏度。这可以用作早期感染中登革热确诊的诊断工具。

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