首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Comparisons of standard curve-fitting methods to quantitate Neisseria meningitidis group A polysaccharide antibody levels by enzyme-linked immunosorbent assay.
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Comparisons of standard curve-fitting methods to quantitate Neisseria meningitidis group A polysaccharide antibody levels by enzyme-linked immunosorbent assay.

机译:通过酶联免疫吸附测定法定量脑膜炎奈瑟氏球菌A组多糖抗体水平的标准曲线拟合方法的比较。

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摘要

We examined several of the more commonly used models (log-log, two forms of the logit-log, and the four-parameter logistic-log transformations) for forming standard or calibration curves by using a standardized enzyme-linked immunosorbent assay (ELISA). Assay range, accuracy, and error for each function were measured and compared. Antibody levels to Neisseria meningitidis group A polysaccharide were estimated by calculating antibody concentrations of a serially diluted standard reference serum of known concentration. Each function achieved a high squared correlation coefficient (r2 greater than 0.97), indicating a high degree of accuracy in forming the standard curves. However, when predicted antibody concentrations were compared with the known values, the log-log function exhibited the least precision, with extreme percentages of error occurring at several dilutions. A partially specified logit-log transformation performed better than the log-log model over a reduced range of standard dilutions. This indicated that a high r2 alone was not a reliable measure of the accuracy of the standard curve. Of the methods surveyed, the logistic-log and fully specified logit-log functions were the most accurate models for forming standard curves and for interpolating antibody concentrations from the standard curve. The accuracy of the fully specified logit-log function is highly dependent on the precise specification of two unknown quantities, the optical densities at zero and infinite concentrations, prior to fitting the model to a typical set of calibration data. The four-parameter logistic-log function was the preferred choice for quantitating N. meningitidis group A total polysaccharide antibody by using a standardized ELISA. The function does not require prespecification of any parameters before estimating the standard curve, and the four parameters are readily interpretable in terms of identifiable physical quantities. This model also has the advantage that it is easiest to visualize since it does not incorporate complex transformations of the optical density scale.
机译:我们使用标准化的酶联免疫吸附测定(ELISA)检查了几种更常用的模型(对数对数,两种形式的对数对数和四参数对数对数转换)以形成标准或校准曲线。测量并比较每个功能的测定范围,准确性和误差。通过计算已知浓度的系列稀释标准参考血清的抗体浓度来估算针对脑膜炎奈瑟氏球菌A组多糖的抗体水平。每个函数都具有较高的平方相关系数(r2大于0.97),表明在形成标准曲线时具有很高的准确性。但是,将预测的抗体浓度与已知值进行比较时,对数-对数函数显示的精度最低,在几种稀释度下出现极高的误差百分比。在缩小的标准稀释范围内,部分指定的对数-对数变换的性能优于对数-对数模型。这表明仅高r2不能可靠地衡量标准曲线的准确性。在所调查的方法中,逻辑对数和完全指定的对数对数函数是形成标准曲线和从标准曲线内插抗体浓度的最准确模型。在将模型拟合到一组典型的校准数据之前,完全指定的对数-对数函数的精度高度依赖于两个未知量(零和无限浓度下的光密度)的精确规格。四参数对数对数函数是通过使用标准化ELISA定量脑膜炎奈瑟氏球菌A组总多糖抗体的首选选择。在估算标准曲线之前,该功能不需要预先指定任何参数,并且可以根据可识别的物理量轻松解释这四个参数。该模型还具有最容易可视化的优点,因为它没有包含光密度标度的复杂变换。

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