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首页> 外文期刊>Journal of Virological Methods >The establishment and clinical evaluation of a novel, rapid, no-wash one-step immunoassay for the detection of dengue virus non-structural protein 1
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The establishment and clinical evaluation of a novel, rapid, no-wash one-step immunoassay for the detection of dengue virus non-structural protein 1

机译:一种新型,快速,无洗涤一步免疫测定的建立和临床评价,用于检测登革病毒非结构蛋白1

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摘要

Dengue fever is a highly endemic arthropod-borne viral disease in the tropical and sub-tropical countries and is rapidly becoming a global threaten. Diagnosis has been conducted by either traditional serological methods or molecular biological techniques. However, these methods are either labor-intensive, time-consuming or with multiple steps, which are not suitable for high throughput detection of large quantity of samples. In the current study, a novel, rapid, no-wash one-step amplified luminescent proximity homogenous assay-linked immunosorbent assay (AlphaLISA) was developed and optimized for the diagnosis of dengue fever through the detection of dengue virus non-structural protein 1 (NS1). The linear range of the assay was determined to be 60,000 pg/mL to 200 pg/mL, with a lower detection limit of 127.45 pg/mL for NS1 protein. The precision of the assay was 8.24 % and 4.93 % for the high and low concentration. Clinical evaluation indicated that the sensitivity and specificity of the assay was 91.49 % and 81.54 %, respectively. This novel, rapid, no-wash one-step AlphaLISA assay is convenient and sensitive, which could be a good alternative for the screening of dengue fever in a high throughput format.
机译:登革热是热带和亚热带国家的高度特有的节肢动物病毒疾病,并迅速成为全球威胁。通过传统的血清学方法或分子生物学技术进行了诊断。然而,这些方法是劳动密集型,耗时或具有多个步骤,其不适用于大量样品的高通量检测。在目前的研究中,开发了一种新颖的,快速的无洗涤的一步扩增的发光邻近均匀的测定链致免疫吸附测定(Alphalisa),并通过检测登革热病毒非结构蛋白1来诊断登革热( ns1)。测定的线性范围测定为60,000pg / ml至200pg / ml,检测限为NS1蛋白的127.45pg / ml。测定的精度为高浓度和低浓度为8.24%和4.93%。临床评价表明,分别的敏感性和特异性分别为91.49%和81.54%。这部小说,快速,无洗净一步的alphalisa测定是方便且敏感的,这可能是以高通量格式筛选登革热的替代方案。

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