Carle G F, Olson M V
Nucleic Acids Res. 1984 Jul 25;12(14):5647-64. doi: 10.1093/nar/12.14.5647.
A simple agarose-gel apparatus has been developed that allows the separation of DNA molecules in the size range from 50 kb to well over 750 kb, the largest size for which size standards were available. The apparatus is based on the recent discovery that large DNA molecules are readily fractionated on agarose gels if they are alternately subjected to two approximately orthogonal electric fields. The switching time, which was on the order of 20-50 sec in our experiments, can be adjusted to optimize fractionation in a given size range. The resolution of the technique is sufficient to allow the fractionation of a sample of self-ligated lambda DNA into a ladder of approximately 15 bands, spaced at 50 kb intervals. We have applied the technique to the fractionation of yeast DNA into 11 distinct bands, several of which have been shown by DNA-DNA hybridization to hybridize uniquely to different chromosome-specific hybridization probes. In this paper, we describe the design of the apparatus, the electrophoretic protocol, and the sample-handling procedures that we have employed.
已开发出一种简单的琼脂糖凝胶装置,它能够分离大小在50 kb至远超750 kb范围内的DNA分子,750 kb是现有大小标准下的最大尺寸。该装置基于最近的一项发现,即如果让大的DNA分子交替经受两个近似正交的电场,它们就能在琼脂糖凝胶上轻松分级分离。在我们的实验中,切换时间约为20 - 50秒,可进行调整以优化给定大小范围内的分级分离。该技术的分辨率足以将自连接的λDNA样品分级分离成约15条带的梯状图谱,条带间隔为50 kb。我们已将该技术应用于将酵母DNA分级分离成11条不同的带,通过DNA - DNA杂交已表明其中几条带分别与不同的染色体特异性杂交探针独特杂交。在本文中,我们描述了所使用的装置设计、电泳方案及样品处理程序。