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首页> 外文期刊>Journal of Virological Methods >Validation of a luminescence immunoassay for the detection of PrP(Sc) in brain homogenate.
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Validation of a luminescence immunoassay for the detection of PrP(Sc) in brain homogenate.

机译:用于检测脑匀浆中PrP(Sc)的发光免疫测定法的验证。

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摘要

A luminescence immunoassay (LIA) was developed for the diagnosis of bovine spongiform encephalopathy (BSE) in brain tissue using two different monoclonal antibodies for capture and detection of the protease-resistant fragment of the pathological prion protein (PrP27-30). PrP27-30 currently represents the most reliable marker for the infectious particle (denominated prion) causing transmissible spongiform encephalopathies (TSEs). Internal and official validation studies of this assay are described using brain homogenates from ascertained BSE positive and negative cows. Using more than 300 positive and 1400 negative bovine or ovine samples, an excellent sensitivity and specificity of 100% were demonstrated. More than 1000-fold dilutions of a BSE positive homogenate still resulted in a clear positive signal. In combination with a simple homogenisation procedure for the preparation of the samples, this assay lends itself for large scale screening of cattle and sheep for TSEs using complete automation of the process.
机译:开发了一种发光免疫测定法(LIA),用于诊断脑组织中的牛海绵状脑病(BSE),使用了两种不同的单克隆抗体来捕获和检测病理性pr病毒蛋白(PrP27-30)的蛋白酶抗性片段。 PrP27-30目前代表引起传染性海绵状脑病(TSE)的传染性颗粒(称为病毒)的最可靠标记。使用确定的BSE阳性和阴性母牛的脑匀浆描述了此测定法的内部和官方验证研究。使用300多个阳性和1400个阴性牛或绵羊样品,证明了100%的出色灵敏度和特异性。 BSE阳性匀浆的1000倍以上稀释仍产生清晰的阳性信号。结合简单的均质化方法来制备样品,该测定法非常适合使用完全自动化的流程对牛和绵羊的TSE进行大规模筛选。

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