Das J, Baese H J
Biochemisches Institut, Medizinischen Fakultät, Christian-Albrechts-Universität Kiel, Federal Republic of Germany.
Anal Biochem. 1987 Jul;164(1):175-80. doi: 10.1016/0003-2697(87)90383-6.
The method for two-dimensional gel electrophoresis of J. Klose and M. Feller [(1981) Electrophoresis 2, 12-24] has been simplified by reducing the thickness of the gels from 3.5 to 1.1 mm for isoelectric focusing gels and from 3.5 to 0.84 mm for sodium dodecyl sulfate slab gels. Thin gels need less reagents and smaller sample volumes. Cooling of the thin gels during electrophoresis is more effective, which allows the use of higher electric power. Therefore, less time is required for an electrophoretic run (approx 4 h). The resolution increases due to the smaller size of the spots. The time required for staining the gels is reduced from at least 3 days to about 1 h. The method has been tested with a protein sample from the filamentous fungus Fusarium solani.
J. 克洛泽和M. 费勒(1981年,《电泳》第2卷,第12 - 24页)的二维凝胶电泳方法已得到简化,等电聚焦凝胶的厚度从3.5毫米减至1.1毫米,十二烷基硫酸钠平板凝胶的厚度从3.5毫米减至0.84毫米。薄凝胶所需试剂更少,样品体积更小。电泳过程中对薄凝胶进行冷却更有效,这使得可以使用更高的电功率。因此,电泳运行所需时间更短(约4小时)。由于斑点尺寸更小,分辨率提高。凝胶染色所需时间从至少3天减少到约1小时。该方法已用丝状真菌茄病镰刀菌的蛋白质样品进行了测试。