Ofverstedt L G, Hammarström K, Balgobin N, Hjertén S, Pettersson U, Chattopadhyaya J
Biochim Biophys Acta. 1984 Jun 16;782(2):120-6. doi: 10.1016/0167-4781(84)90014-9.
The use of displacement electrophoresis (synonymous to isotachophoresis, steady-state stacking, and moving boundary electrophoresis) for recovery of DNA fragments from agarose and polyacrylamide gels is described. Complete recovery of DNA molecules ranging from oligonucleotides to 20 000-basepairs-long fragments was achieved. The DNA is recovered in a small volume (0.1-0.3 ml) and can be used directly in enzyme-mediated cleavage and ligation reactions. The recovered DNA contained no inhibitory contaminants as revealed by ligation or restriction enzyme cleavage.
本文描述了使用置换电泳(等同于等速电泳、稳态堆积和移动边界电泳)从琼脂糖凝胶和聚丙烯酰胺凝胶中回收DNA片段的方法。实现了从寡核苷酸到20000碱基对长片段的DNA分子的完全回收。回收的DNA体积小(0.1 - 0.3毫升),可直接用于酶介导的切割和连接反应。连接或限制性内切酶切割结果显示,回收的DNA不含抑制性污染物。