Kasatiya S S, Lambert N G, Laurence R A
Appl Microbiol. 1974 May;27(5):838-43. doi: 10.1128/am.27.5.838-843.1974.
A pulsed dye laser was used as an excitation source in a fluorescent treponemal antibody absorption (FTA-ABS) test. A high precision in quantitative fluorescence was obtained with this high-power excitation source coupled to an electronic detection system and a storage oscilloscope by standardization of fluorescence evaluation and through elimination of human error. One 0.4-mus pulse exposure was sufficient to record fluorescence intensity data on the oscilloscope. Absence of fading of fluorescence after repeated excitation permitted multiple readings of the same microscope field. Almost 100% reproducible results were obtained for the FTA-ABS test with 40 samples. Electronic detection of fluorescence and the high sensitivity obtained with laser excitation raise doubts about the relative value of quantitative immunofluorescence in the FTA-ABS test.
在荧光密螺旋体抗体吸收(FTA - ABS)试验中,脉冲染料激光器被用作激发源。通过荧光评估的标准化以及消除人为误差,将这种高功率激发源与电子检测系统和存储示波器相结合,获得了高精度的定量荧光。一次0.4微秒的脉冲曝光足以在示波器上记录荧光强度数据。反复激发后荧光不褪色,使得可以对同一显微镜视野进行多次读数。对40个样本进行FTA - ABS试验,结果几乎100%可重复。荧光的电子检测以及激光激发所获得的高灵敏度,让人对FTA - ABS试验中定量免疫荧光的相对价值产生怀疑。