Nöhammer G
Histochemistry. 1984;80(4):395-400. doi: 10.1007/BF00495424.
Conditions are described by which cells and fresh frozen tissues, following fixation with ethanol-ether, and after staining with the amidoblack (AB)-TCA-staining method, show a modified dye/protein ratio of 0.9 moles AB/10(5) g protein compared to 8.5 moles AB/10(5) g protein ( Schauenstein et al. 1980) as in a previously used method. In contrast to the AB-TCA-method, which leads to extremly high and unmeasurable extinctions in tissue sections, staining with the modified AB-TCA- 23st -method with 10 microns tissue sections produces easily measurable extinction values. A correlation of the microspectrometrically determined mean total extinction values of different cell types and nuclei after staining with the tetrazonium method (N ohammer 1978; N ohammer and Desoye 1981) and on the other hand with the AB-TCA 23st -method has been found. The microspectrometrically determined extinctions after AB-TCA 23st -staining can be calculated; an extinction of 0.04248 corresponds to 1 pgm protein.
细胞和新鲜冷冻组织在用乙醇 - 乙醚固定后,采用氨基黑(AB)-三氯乙酸(TCA)染色法染色,与之前使用的方法相比,染料/蛋白质的比例有所改变,为0.9摩尔AB/10⁵克蛋白质,而之前的方法该比例为8.5摩尔AB/10⁵克蛋白质(绍恩施泰因等人,1980年)。与AB - TCA方法不同,AB - TCA方法会导致组织切片出现极高且无法测量的吸光度,而用改良的AB - TCA - 23st方法对10微米厚的组织切片染色,则可轻松获得可测量的吸光度值。已发现,用四氮唑法(诺哈默,1978年;诺哈默和德索耶,1981年)染色后,通过显微分光光度法测定的不同细胞类型和细胞核的平均总吸光度值,与用AB - TCA 23st方法测定的吸光度值之间存在相关性。用AB - TCA 23st染色后通过显微分光光度法测定的吸光度可以进行计算;吸光度为0.04248相当于1皮克蛋白质。