Abstract
Although Hb-C may be separated from Hb A2 by some ion exchange methods, most will not separate Hb E and Hb A2. The δ chain can be readily separated from the βc, βE and βO–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 β-that heterozygotes and, therefore, is applicable to other conditions (Hb C, Hb E, Hb O-Arab).