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Development of an enhanced chemiluminescence immunoassay (CLIA) for detecting urinary albumin

机译:用于检测尿白蛋白的增强型化学发光免疫分析法(CLIA)的开发

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In the present study, a sensitive and competitive chemiluminescence immunoassay (CLIA) was developed in order to detect human serum albumin (HSA) in urine specimen. The method utilizes a home-made monoclonal anti-albumin antibody conjugated to horseradish peroxidase enzyme (mAb-HRP). Sensitivity, specificity and linearity of the assay were evaluated. According to the results, the proper concentration of HSA and mAb-HRP conjugates was 800 ng/100 μl and 1:200 respectively. In optimal conditions, this method could detect HSA in a high linear range of 10–200 μg ml1 with the low detection limit of 0.025 μg ml1. No evidence of interference with presence of probable substances in the urine samples indicated its high specificity and selectivity. Moreover, high reproducibility as well as high sensitivity and specificity of the test were confirmed using diabetic and non-diabetic samples. Significant concordance was observed between CLIA and immunoturbidimetry assay regarding detection of HSA. The results of the present study can be considered in accordance with the current demands such as reliability, accuracy, convenience and high speed of performance for a precise protein detection method. Furthermore, it may be regarded as a more rapid, simpler and cheaper alternative compared to other sophisticated assays.
机译:在本研究中,为了检测尿液样本中的人血清白蛋白(HSA),开发了一种灵敏且竞争性的化学发光免疫分析法(CLIA)。该方法利用偶联至辣根过氧化物酶(mAb-HRP)的自制单克隆抗白蛋白抗体。评价了测定的灵敏度,特异性和线性。根据结果​​,HSA和mAb-HRP缀合物的适当浓度分别为800 ng / 100μl和1:200。在最佳条件下,此方法可以在10-200μgml1的高线性范围内检测HSA,而下限为0.025μgml1。没有证据表明尿液样品中可能存在的物质受到干扰,表明其高特异性和选择性。而且,使用糖尿病和非糖尿病样品证实了测试的高重复性以及高灵敏度和特异性。在CLIA和免疫比浊法检测之间就HSA的检测发现存在显着一致性。可以根据当前的需求,例如精确蛋白质检测方法的可靠性,准确性,便利性和高性能,来考虑本研究的结果。此外,与其他复杂的分析方法相比,它可以被认为是更快速,更简单,更便宜的替代方法。

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