Love John L, Scholes Paula, Gilpin Brent, Savill Marion, Lin Susan, Samuel Laly
Christchurch Science Centre, Institute of Environmental Science and Research Ltd., PO Box 29 181, Christchurch, New Zealand.
J Microbiol Methods. 2006 Nov;67(2):349-56. doi: 10.1016/j.mimet.2006.04.005. Epub 2006 Jun 2.
Quantitative real-time PCR is one of the newer methods for measurement of the amount of nucleic material in biological systems. However, reliable measurement requires an appropriate estimation of uncertainty and this paper has developed the uncertainty budget associated with this procedure using as an example, data from a quantitative real-time PCR method for the enumeration of Campylobacter jejuni. This uncertainty is relatively large and for instance, a measured result of 151 units of DNA would have a 95% confidence interval of +/-84 units of DNA with the main sources of uncertainty being the measurement of the threshold cycle (Ct) value, the predicted DNA content of the unknown sample from the calibration line and the molar absorbance value for DNA.
定量实时聚合酶链反应(Quantitative real-time PCR)是测量生物系统中核酸物质含量的较新方法之一。然而,可靠的测量需要对不确定度进行适当估计,本文以空肠弯曲菌定量实时PCR计数法的数据为例,制定了与该程序相关的不确定度预算。这种不确定度相对较大,例如,151个DNA单位的测量结果在95%置信区间内的不确定度为±84个DNA单位,不确定度的主要来源是阈值循环(Ct)值的测量、校准曲线中未知样品的预测DNA含量以及DNA的摩尔吸光值。