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作 者:王春风[1] 王京芳[1] 李全民[1] 胡秋娈[2]
机构地区:[1]河南师范大学化学与环境科学学院,河南新乡453007 [2]洛阳师范学院化学系,河南洛阳471022
出 处:《化学试剂》2005年第9期541-544,共4页Chemical Reagents
摘 要:研究表明,在pH 1.5的Clark-Lubs(C-L)缓冲介质中,偶氮胂羧与多种蛋白质在室温下能迅速结合生成蓝色复合物,λmax为612nm,线性范围(HSA)为0~100mg/L,表观摩尔吸光系数为2.67×105L·mol-1·cm-1.研究了光谱性质及反应机理,试验了影响因素,在确定的最佳实验条件下,建立了以CAA为光谱探针的光度法测定人血清蛋白质的新方法.测定人血清样品中蛋白质的含量,与经典的考马斯亮蓝G-250法(CBB G-250)结果一致.In pH 1.5 Clark-Lubs buffer, carboxyarsenazo could bind rapidly with many kinds of proteins at room temperature forming a blue complex, which had a maximum absorption wavelength at 612nm. Beer' s law was obeyed in the range from 0 to 100 rag/L(HSA). The molar absorptivity of reaction product was 2.67 × 105L· mol^-1. cm^-1. The influencing factors and mechanism were studied. A new method for the determination of proteins by using carboxyarsenazo as a spectral probe was established under the optimal conditions. This method has been used for the determination of total protein in human serum samples. The results obtained agreed well with those by coomassie brilliant blue G-250 method.
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