Kainz P, Kainz V
Department of Biochemistry, University of Salzburg, Austria.
Anal Biochem. 1989 May 1;178(2):260-2. doi: 10.1016/0003-2697(89)90635-0.
Nick translation of DNA bound to nylon membranes is described. Phage lambda DNA was digested with restriction endonuclease HindIII. The fragments were separated by agarose electrophoresis and electrophoretically transferred to Zeta-Probe nylon membranes. After being air-dried, the areas with DNA fragments attached were cut out and subjected to nick translation. The labeled fragments, removed from the membranes by a single wash step, can be used as specific hybridization probes. Currently used methods require time-consuming electroelution and often additional purification procedures if a specific DNA fragment, separated by gel electrophoresis, is to be labeled by nick translation. With the procedure described it is possible to label many DNA fragments in parallel in a time- and cost-saving manner.
本文描述了与尼龙膜结合的DNA的切口平移法。用限制性内切酶HindIII消化噬菌体λDNA。片段通过琼脂糖电泳分离,然后电泳转移到Zeta-Probe尼龙膜上。空气干燥后,切下附着有DNA片段的区域并进行切口平移。通过单次洗涤步骤从膜上洗脱下来的标记片段可作为特异性杂交探针。如果要通过切口平移标记经凝胶电泳分离的特定DNA片段,目前使用的方法需要耗时的电洗脱,且通常还需要额外的纯化步骤。采用本文所述方法,可以省时省钱地并行标记多个DNA片段。