Van der Ploeg M, Van den Broek K, Mitchell J P
Histochemistry. 1979 Jul;62(1):29-43. doi: 10.1007/BF00537004.
A computer program has been developed for stage-scanning cytophotometry of double-stained microscopical specimens. The program permits the simultaneous measurement of absorbance values at two wavelengths in each measuring spot. To account for overlap in the absorbance spectra of the two stained endproducts, the program incorporates correction of the measured data to compensate for the contribution of each chromophore to the absorbance measured for the other. The program will compute the corrected local absorbance values at specified wavelengths for each chromophore at each measuring spot and integrate these values over the total object to give separate totals for each stain. It is also possible to have integrated the absorbance values of one chromophore for all those measuring spots where the local corrected absorbance value of the other chromophore exceeds a preset minimum value. When this other chromophore is a nuclear DNA stain, it is possible to obtain an approximate measure of the content of any compound in the nuclear area which can be stained with a chromophore having an absorbance spectrum different from the DNA stain. The validity of the program was investigated on model preparations consisting of two (differently) coloured films of which the absorbance values could be measured either individually or in combination, by partially overlaying one film on the other. The program's potential has been demonstrated by using the combination of either Naphthol Yellow S or dinitrofluorobenzene as protein stains with the Feulgen-pararosaniline(SO2) procedure for DNA in chicken erythrocytes and rat liver cells.
已开发出一种用于双染色显微镜标本阶段扫描细胞光度测定的计算机程序。该程序允许在每个测量点同时测量两个波长处的吸光度值。为了考虑两种染色终产物吸光光谱的重叠,该程序对测量数据进行校正,以补偿每种发色团对另一种发色团测量吸光度的贡献。该程序将计算每个测量点每种发色团在指定波长处的校正局部吸光度值,并将这些值在整个物体上积分,以给出每种染色剂的单独总量。还可以对所有那些另一种发色团的局部校正吸光度值超过预设最小值的测量点,对一种发色团的吸光度值进行积分。当这种另一种发色团是核DNA染色剂时,就有可能获得核区域中任何可用具有与DNA染色剂不同吸光光谱的发色团染色的化合物含量的近似测量值。通过由两片(不同)颜色的薄膜组成的模型制剂对该程序的有效性进行了研究,其中薄膜的吸光度值可以单独测量或组合测量,方法是将一片薄膜部分覆盖在另一片薄膜上。通过使用萘酚黄S或二硝基氟苯作为蛋白质染色剂与用于鸡红细胞和大鼠肝细胞中DNA的福尔根-副品红(SO2)程序相结合,证明了该程序的潜力。