Blokhin Russian Cancer Research Center, Russian Academy of Medical Sciences, Moscow, Russia.
Biochemistry (Mosc). 2009 Nov;74(11):1285-8. doi: 10.1134/s0006297909110169.
A new method of electrophoresis (isotachophoresis in agarose gel rods) in which nucleic acid molecules are not separated but, oppositely, are brought together into one band, was elaborated. Heterogeneous in size DNA and RNA polymers present in a few milliliters of a solution at so low concentration that their isolation by other methods is hardly attainable and fraught with losses are brought together into one visible narrow band when put in a discontinuous electric field. Polynucleotides migrate in dilute (0.1%) semifluid agarose gel that permits easy quantitative isolation of the band of interest. Resulting DNA can be used directly in PCR. The suggested method for isolation of micro amounts of nucleic acids from dilute solutions can be applied to forensic and clinical research and cancer gene diagnostics by the analysis of fragmented circulating DNA from bodily fluids.
一种新的电泳方法(琼脂糖凝胶棒中的等速电泳),其中核酸分子不是分离的,而是相反地聚集在一起形成一条带。在几毫升溶液中,大小不均的 DNA 和 RNA 聚合物的浓度非常低,用其他方法分离几乎不可能,而且容易丢失。当置于不连续电场中时,它们聚集在一条可见的窄带中。多核苷酸在稀(0.1%)半流动琼脂糖凝胶中迁移,便于轻松定量分离感兴趣的条带。所得 DNA 可直接用于 PCR。从稀溶液中分离微量核酸的建议方法可应用于法医和临床研究以及通过分析体液中循环的断裂 DNA 进行癌症基因诊断。