Naoum P C, Teixeira U A, de Abreu Machado P E, Michelin O C
Rev Bras Pesqui Med Biol. 1978 Oct;11(4-5):241-4.
Human oxyhaemoglobin A and A2 from normal individuals and oxyhaemoglobin S from patients with sickle cell anaemia and sickle cell trait were studied using Isopropanol/buffer method at 37 degrees C and 40 degrees C. Hb S was less stable than Hb A, whereas Hb A2 was considerably more stable than either. Denaturation of Hb S was dependent on temperature and its concentration. Between the patients with sickle cell trait it was not possible to verify the influence of the concentration probably due to the small range used (from 38% to 44%).
采用异丙醇/缓冲液法,在37摄氏度和40摄氏度下,对来自正常个体的人血红蛋白A和A2以及镰状细胞贫血和镰状细胞性状患者的血红蛋白S进行了研究。血红蛋白S比血红蛋白A稳定性差,而血红蛋白A2比两者都稳定得多。血红蛋白S的变性取决于温度及其浓度。在镰状细胞性状患者中,由于所用浓度范围较小(从38%到44%),无法验证浓度的影响。