Kaiho S, Mizuno K
Anal Biochem. 1985 Aug 15;149(1):117-20. doi: 10.1016/0003-2697(85)90483-x.
Sensitive and rapid assays, colorimetry and histochemistry, for hemoglobin in erythroid cells are established. The assays are based on pseudoperoxidase activity of hemoglobin using 2,7-diaminofluorene as a hydrogen donor for the peroxidase, instead of benzidine which is widely benzidine which is widely used for the detection of small amounts of hemoglobin but which is a potent carcinogen and has been banned from laboratory use. In the presence of hydrogen peroxide, hemoglobin catalyzes the formation of a blue compound (fluorene blue), which has a broad absorption band between 500 and 690 nm with a peak at 610 nm, from 2,7-diaminofluorene. The reagent is safe to use in the laboratory. The methods could be applied to the detection of hemoglobin in Friend erythroleukemia cells induced to cell differentiation along the erythroid pathway by dimethyl sulfoxide.
已建立用于检测红系细胞中血红蛋白的灵敏且快速的检测方法,即比色法和组织化学法。这些检测方法基于血红蛋白的拟过氧化物酶活性,使用2,7 - 二氨基芴作为过氧化物酶的氢供体,而非广泛用于检测少量血红蛋白但却是强致癌物且已被禁止在实验室使用的联苯胺。在过氧化氢存在的情况下,血红蛋白催化由2,7 - 二氨基芴形成一种蓝色化合物(芴蓝),该化合物在500至690nm之间有一个宽吸收带,峰值在610nm。该试剂在实验室使用安全。这些方法可应用于检测经二甲基亚砜诱导沿红系途径进行细胞分化的弗氏红白血病细胞中的血红蛋白。