Robertson W R, Davison B, Gandy M, Burdge R, Lambert A
Histochem J. 1984 Jun;16(6):651-6. doi: 10.1007/BF01003392.
An experimental set-up for the continuous monitoring of cytochemical enzyme reaction rates is described. The design consists of a 32K Commodore PET microcomputer, upgraded to Basic 4 and containing a graphics facility. The microcomputer is interfaced with a Vickers M85A microdensitometer, which has been modified and equipped with a Zeiss X63 water immersion objective. The software allows for the automatic transfer of density readings from the M85A to the microcomputer, and for the continuous monitoring of the enzyme reaction as its proceeds at short time intervals (i.e. down to 3.3 s). The relationship between the absorbance change of the enzyme final reaction product and time is printed both numerically and graphically. Initial velocity rates are calculated by regression analysis, and statistical evaluation of grouped data is possible.
本文描述了一种用于连续监测细胞化学酶反应速率的实验装置。该装置由一台32K的Commodore PET微型计算机组成,已升级到Basic 4版本并具备图形功能。微型计算机与一台经过改装并配备蔡司X63水浸物镜的维氏M85A显微密度计相连。该软件可实现将M85A的密度读数自动传输到微型计算机,并能在短时间间隔(即低至3.3秒)内持续监测酶反应的进行情况。酶最终反应产物的吸光度变化与时间的关系以数字和图形方式打印出来。通过回归分析计算初始速度率,并且可以对分组数据进行统计评估。