Snyder D B, Marquardt W W, Mallinson E T, Allen D A, Savage P K
Vet Immunol Immunopathol. 1985 Aug;9(4):303-17. doi: 10.1016/0165-2427(85)90061-3.
A model enzyme-linked immunosorbent assay (ELISA) system was developed which permits the user to evaluate replicate single sera dilutions of 46 test and control serum samples for the presence of specific antibody against up to eight different antigens in one assay. The system makes use of a transplanting device for the simultaneous transfer of aliquots of independently diluted replicate test samples along with conjugate and substrate from a serum reservoir plate or from a reagent reservoir onto different antigen coated target plates. Kinetically read, raw absorbance data from tests are transmitted to a microcomputer, where absorbance values from all tests are quickly reduced to predicted titer levels by computer analysis. All titer computations involve the use of a single prescribed standard curve for predicting antibody titer against the different antigens. Between assay repeatability of this procedure is high and its potential for replacing a number of different conventional assays for epidemiological studies has been evaluated.
开发了一种酶联免疫吸附测定(ELISA)系统,该系统可让用户在一次测定中评估46个测试和对照血清样本的重复单血清稀释液中是否存在针对多达八种不同抗原的特异性抗体。该系统利用一种移液装置,将独立稀释的重复测试样本的等分试样与结合物和底物同时从血清储存板或试剂储存器转移到不同的抗原包被靶板上。对测试的原始吸光度数据进行动力学读取,并传输到微型计算机,在计算机分析下,所有测试的吸光度值迅速换算为预测滴度水平。所有滴度计算均使用单一规定标准曲线来预测针对不同抗原的抗体滴度。该方法的批内重复性很高,并且已经评估了其在流行病学研究中替代多种不同传统检测方法的潜力。