单纯疱疹病毒1型抗原、游离抗原和细胞结合抗原的ELISA定量测定和可视化。

R Tirado, R E Sarmiento, B Gómez
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引用次数: 0

摘要

描述了一种通过间接酶联免疫吸附试验(ELISA)定量和可视化单纯疱疹病毒1型抗原的方法。该试验通过使用多克隆血清来简化,并且可以应用于游离抗原以及细胞结合的定量。此外,细胞病毒抗原可以可视化。抗原来源为病毒悬浮液、感染细胞和从感染细胞中提取的蛋白。该试验具有特异性,其敏感性取决于抗原来源。在抗原浓度与净吸光度值(病毒抗原减去对照抗原所得吸光度之差)直接相关(r > 0.8)的范围内,该技术被认为是特异性的。与其他ELISA方法相比,该技术具有优势:不需要单克隆抗体,或标记抗病毒免疫球蛋白或来自两种不同物种的抗病毒血清。此外,还可测定游离抗原总量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative determination and visualization of herpes simplex virus type 1 antigen, free and cell-bound by ELISA.

A method of quantifying and visualizing herpes simplex virus type 1 antigen by indirect enzyme-linked immunosorbent assay (ELISA) is described. This assay is simplified by the use of polyclonal serum and can be applied to the quantification of free antigen as well cell-bound. Moreover, cell viral antigen can be visualized. Antigen sources were viral suspensions, infected cells and proteins extracted from infected cells. The assay was specific and its sensitivity was dependent on the antigen source. The technique was regarded as specific within a range showing a direct correlation (r > 0.8) between the concentration of the antigen and the net absorbance value (the difference of the absorbance obtained with the viral antigen minus the control antigen). The technique has advantages over other ELISA procedures: does not require monoclonal antibodies, or labelled antiviral immunoglobulins or antiviral serum from two different species. In addition total free antigen can be measured.

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