Schroeder W A, Shelton J B, Shelton J R, Huynh V
Hemoglobin. 1986;10(3):253-7. doi: 10.3109/03630268609042846.
Although Hb-C may be separated from Hb A2 by some ion exchange methods, most will not separate Hb E and Hb A2. The delta chain can be readily separated from the beta C, beta E and beta O-Arab chains by reverse phase HPLC. Hence, reverse phase HPLC provides a means of quantitatively determining Hb A2 in the presence of Hb C, Hb E, and Hb O-Arab. The procedure, although not highly accurate, does permit the detection of increased Hb A2, for example, in beta-thal heterozygotes and, therefore, is applicable to other conditions (Hb C, Hb E, Hb O-Arab).
虽然通过一些离子交换方法可将血红蛋白C(Hb-C)与血红蛋白A2(Hb A2)分离,但大多数方法无法分离血红蛋白E(Hb E)和Hb A2。通过反相高效液相色谱法(reverse phase HPLC)可轻松将δ链与βC、βE和βO-阿拉伯链分离。因此,反相高效液相色谱法提供了一种在存在Hb C、Hb E和Hb O-阿拉伯血红蛋白的情况下定量测定Hb A2的方法。该方法虽然不够精确,但确实能够检测到Hb A2的增加,例如在β地中海贫血杂合子中,因此适用于其他情况(Hb C、Hb E、Hb O-阿拉伯血红蛋白)。