Marlow S J, Handa A K
J Immunol Methods. 1987 Jul 16;101(1):133-9. doi: 10.1016/0022-1759(87)90226-2.
The use of a recently available commercial membrane (Immunodyne Immunoaffinity), which covalently binds proteins, in the development of a quantitative immunological slot blot assay is demonstrated. This membrane was found to be valuable in the quantification of polygalacturonase from tomato fruit, a protein which binds weakly to nitrocellulose membrane. The covalent binding of protein to a solid support allows the use of stringent conditions necessary for reduction of non-specific interactions between antibodies and other proteins. This method should prove useful to develop quantitative immunoassays for proteins which elute from nitrocellulose or other membranes during assay conditions.
本文展示了一种最近可得的商业膜(免疫亲和免疫膜)在定量免疫斑点印迹分析方法开发中的应用,该膜能与蛋白质共价结合。已发现这种膜对于定量分析番茄果实中的多聚半乳糖醛酸酶很有价值,多聚半乳糖醛酸酶是一种与硝酸纤维素膜结合较弱的蛋白质。蛋白质与固相支持物的共价结合使得可以使用严格条件,以减少抗体与其他蛋白质之间的非特异性相互作用。该方法对于开发针对在分析条件下从硝酸纤维素或其他膜上洗脱的蛋白质的定量免疫分析应是有用的。