Callus B A, Busfield S J, Klinken S P
Department of Biochemistry, University of Western Australia, Nedlands.
Hemoglobin. 1995 Jan-Mar;19(1-2):7-19. doi: 10.3109/03630269509069725.
We have used the diaminofluorene stain to detect hemoglobin production in J2E cells following erythropoietin-induced differentiation. The pseudo-peroxidase activity of hemoglobin produces a colored product, fluorene blue, which can be measured spectrophotometrically. We found that the absorbance varied with time and concentration of hemoglobin, making it unsuitable for rapid, routine use. However, hemoglobin content could be determined from the initial reaction rate and this correlated extremely well with the number of benzidine positive cells. When used as a direct cytochemical stain diaminofluorene was shown to be more sensitive than benzidine in detecting hemoglobin-producing J2E cells.
我们使用二氨基芴染色法来检测促红细胞生成素诱导分化后的J2E细胞中的血红蛋白生成情况。血红蛋白的假过氧化物酶活性会产生一种有色产物——芴蓝,可通过分光光度法进行测量。我们发现吸光度会随血红蛋白的时间和浓度变化,这使其不适用于快速、常规使用。然而,血红蛋白含量可以根据初始反应速率来确定,并且这与联苯胺阳性细胞的数量高度相关。当用作直接细胞化学染色时,二氨基芴在检测产生血红蛋白的J2E细胞方面比联苯胺更敏感。