Murdock P J, Brooks S, Mellars G, Cheung G, Jacob D, Owens D L, Parmar M, Riddell A
Diagnostic Laboratory, Roy Free Hampstead NHS Trust, Royal Free Hospital, London, UK.
Clin Lab Haematol. 1997 Jun;19(2):111-4. doi: 10.1046/j.1365-2257.1997.00056.x.
A simple monoclonal antibody based ELISA for free Protein S, compatible with out existing ELISA for total Protein S has been developed, and its performance compared with the conventional PEG precipitation method of free Protein S assay. The normal range (mean +/- 2 SD) was 0.19-0.54 iu/ml free Protein S. The mean intra assay variation was 5.24% and the mean inter assay variation was 5.50%. A total of 102 routine diagnostic samples from patients referred for prothrombotic investigation (six assays for each method) were assayed by PEG precipitation (mean 0.32 iu/ml, SD 10.60), and the monoclonal ELISA (mean 0.34, SD 0.9). Paired t-test analysis of the two data sets indicated no significant difference between them (P < 0.001). In this sample population, there was no significant difference in free Protein S values when assayed by monoclonal based ELISA or by PEG precipitation. The monoclonal assay has proved to be reliable, accurate and precise. The monoclonal ELISA is simpler, quicker and easier to perform in routine use. Data generated is directly comparable to that generated by PEG precipitation. This methodology would be suitable for laboratories currently measuring Protein S by ELISA.
已开发出一种基于单克隆抗体的游离蛋白S酶联免疫吸附测定法(ELISA),它与我们现有的总蛋白S ELISA兼容,并将其性能与游离蛋白S测定的传统聚乙二醇沉淀法进行了比较。游离蛋白S的正常范围(平均值±2标准差)为0.19 - 0.54 iu/ml。批内变异均值为5.24%,批间变异均值为5.50%。通过聚乙二醇沉淀法(平均值0.32 iu/ml,标准差10.60)和单克隆ELISA法(平均值0.34,标准差0.9)对总共102例因血栓形成前状态检查而转诊患者的常规诊断样本(每种方法检测6次)进行了检测。对两组数据集进行配对t检验分析表明,它们之间无显著差异(P < 0.001)。在该样本群体中,通过基于单克隆抗体的ELISA法或聚乙二醇沉淀法检测游离蛋白S值时无显著差异。单克隆检测已证明是可靠、准确和精确的。单克隆ELISA法在常规使用中更简单、更快且更易于操作。所生成的数据与聚乙二醇沉淀法生成的数据直接可比。该方法学适用于目前通过ELISA法检测蛋白S的实验室。