Icke G C, Davis R E, Nicol D J
Pathology. 1979 Apr;11(2):169-73. doi: 10.3109/00313027909061942.
A rapid accurate and inexpensive technique for the measurement of haemoglobin A2 has been devised. It uses a small plastic device which embodies a miniature chromatographic column and reservoirs for the eluting buffer and eluates. The device is charged with whole blood, pH 8.25 buffer and centrifuged. The eluate is removed and the centrifugation repeated using pH 7.0 buffer to remove the remaining haemoglobin. The haemoglobin concentration in the 2 volumes of eluates is measured in a spectrophotometer at 414 nm and the percentage of HbA2 calculated. Results are similar to those obtained by standard methods.
已设计出一种快速、准确且廉价的测量血红蛋白A2的技术。它使用一种小型塑料装置,该装置包含一个微型色谱柱以及用于洗脱缓冲液和洗脱液的储液器。将全血、pH 8.25缓冲液装入该装置并进行离心。去除洗脱液,然后使用pH 7.0缓冲液重复离心以去除剩余的血红蛋白。在分光光度计中于414nm处测量两体积洗脱液中的血红蛋白浓度,并计算HbA2的百分比。结果与通过标准方法获得的结果相似。