Arafa M
Department of Microbiology Benha Faculty of Medicine.
J Egypt Public Health Assoc. 1990;65(1-2):49-59.
This technique has been developed for the separation of protein by two-dimensional polyacrylamide gel electrophoresis. Due to its resolution and sensitivity, this technique is a powerful tool for the analysis and detection of proteins from complex biological sources. Proteins were separated according to isoelectric point by isoelectric focusing in the first dimension, and according to molecular weight by sodium dodecyl sulfate electrophoresis in the second dimension. Since these two parameters are unrelated, it is possible to obtain an almost uniform distribution of protein spots across a two-dimensional gel. This technique has resolved about 20 different acidic components from cercarial Ag. So this technique provides a method for estimation of the number of proteins made by any biological system.
这项技术是为通过二维聚丙烯酰胺凝胶电泳分离蛋白质而开发的。由于其分辨率和灵敏度,该技术是分析和检测来自复杂生物来源蛋白质的有力工具。在第一维中通过等电聚焦根据等电点分离蛋白质,在第二维中通过十二烷基硫酸钠电泳根据分子量分离蛋白质。由于这两个参数相互无关,因此有可能在二维凝胶上获得几乎均匀分布的蛋白质斑点。这项技术已从尾蚴抗原中分离出约20种不同的酸性成分。因此,这项技术提供了一种估算任何生物系统产生蛋白质数量的方法。