Manabe T, Hayama E, Okuyama T
Clin Chem. 1982 Apr;28(4 Pt 2):824-7.
In this technique, in which no denaturing agent is used, proteins in human serum, cerebrospinal fluid, and urine are separated by isoelectric focusing in cylindrical 40 g/L polyacrylamide gels of capillary size (1.3 x 35 mm) for 40 min, followed by electrophoresis in 40--170 g/L polyacrylamide linear gradient gel, with use of 38 x 35 x 1 mm slab gel, for 1 h. Only 2 microL of untreated human serum is required to obtain clear protein-distribution patterns, made visible by Coomassie Blue staining. By use of silver staining, proteins in unconcentrated cerebrospinal fluid can be made visible. An apparatus we devised for microscale two-dimensional electrophoresis enables us to analyze eight protein samples simultaneously.
在这项不使用变性剂的技术中,人血清、脑脊液和尿液中的蛋白质先在毛细管尺寸(1.3×35毫米)的40克/升聚丙烯酰胺圆柱形凝胶中进行等电聚焦40分钟,然后在40 - 170克/升聚丙烯酰胺线性梯度凝胶中使用38×35×1毫米的平板凝胶进行电泳1小时。仅需2微升未处理的人血清就能获得清晰的蛋白质分布图谱,通过考马斯亮蓝染色使其可见。使用银染色可使未浓缩的脑脊液中的蛋白质可见。我们设计的一种用于微量二维电泳的仪器能让我们同时分析八个蛋白质样品。