Lüthje J, Ogilvie A
Clin Chim Acta. 1987 May 15;164(3):275-84. doi: 10.1016/0009-8981(87)90302-0.
A method based on native PAGE is used for the quantitative measurement of 5'-nucleotide phosphodiesterase isoenzymes (5'-NPD; EC 3.1.4.1) in human serum. In contrast to other techniques this method works with a commercially available substrate. In sera of healthy donors four isozymes could be separated, designated as 5'-NPD-I, 5'-NPD-II, 5'-NPD-III and 5'-NPD-IV in the reverse order of their electrophoretic mobility. When low amounts of serum were applied to the gel, the separation between all four activities was sufficient enough to allow their quantitation. Higher amounts of serum impaired the separation between the isoenzymes I and II. However, even when using high amounts of serum, the quantitation of these activities was possible when taking advantage of some of their biochemical properties which are described herein.
一种基于非变性聚丙烯酰胺凝胶电泳(native PAGE)的方法用于定量检测人血清中的5'-核苷酸磷酸二酯酶同工酶(5'-NPD;EC 3.1.4.1)。与其他技术不同,该方法使用市售底物。在健康供体的血清中可分离出四种同工酶,按照它们电泳迁移率的相反顺序分别命名为5'-NPD-I、5'-NPD-II、5'-NPD-III和5'-NPD-IV。当向凝胶中加入少量血清时,所有四种活性之间的分离足以进行定量分析。较高量的血清会损害同工酶I和II之间的分离。然而,即使使用大量血清,利用本文所述的一些生化特性仍可对这些活性进行定量分析。