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从凝胶中对寡核苷酸和大片段DNA进行定量电洗脱及通过电渗析进行纯化。

Quantitative electroelution of oligonucleotides and large DNA fragments from gels and purification by electrodialysis.

作者信息

Göbel U, Maas R, Clad A

机构信息

Zentrum für Hygiene, Freiburg, F.R.G.

出版信息

J Biochem Biophys Methods. 1987 Aug;14(5):245-60. doi: 10.1016/0165-022x(87)90050-9.

Abstract

We have designed a new device [Biotrap (Elutrap in the U.S.A. and Canada), available from Schleicher & Schuell] for electroelution, -concentration , and -dialysis of DNA and other charged macromolecules above 5 kDa. In an electric field, the DNA migrates in an open channel out of the gel slice through a microporous membrane, BT2, into the trap section, where it is retained by a very dense, non-adsorbant, and inert membrane BT1. Specifically designed for use in an electric field, the matrix of this new membrane is much denser than that of dialysis membranes. In contrast to dialysis membranes, BT1 will not adsorb large DNA fragments nor allow passage of small DNA fragments when subjected to an electric field. In the absence of an electric field, BT1 and BT2 effectively seal the trap, maintaining the final elution volume of the purified sample. The trap can contain from 200-600 microliter and is collected from above with a pipet. In the experiments described here, 85-95% of oligonucleotides (14-mer) and large (150 kb) DNA fragments were recovered, independent of fragment length. The purity of the eluted DNA was demonstrated by restriction enzyme digestion, nick-translation, primer extension, end-labeling with polynucleotide kinase, and ligation. Electrodialysis was successfully used for the complete removal of common contaminants inhibiting the polynucleotide kinase reaction and for the removal of CsCl from DNA samples.

摘要

我们设计了一种新型装置[Biotrap(在美国和加拿大为Elutrap),可从施莱歇尔&舒尔公司购得],用于DNA及其他分子量大于5 kDa的带电大分子的电洗脱、浓缩和透析。在电场中,DNA在开放通道中从凝胶切片穿过微孔膜BT2迁移到捕集区,在那里它被一层非常致密、非吸附性且惰性的膜BT1截留。这种新型膜的基质专为在电场中使用而设计,比透析膜致密得多。与透析膜不同,BT1在电场作用下不会吸附大的DNA片段,也不会允许小的DNA片段通过。在没有电场的情况下,BT1和BT2有效地密封捕集器,保持纯化样品的最终洗脱体积。捕集器可容纳200 - 600微升,用移液器从上方收集。在此处描述的实验中,85 - 95%的寡核苷酸(14聚体)和大的(150 kb)DNA片段被回收,与片段长度无关。洗脱的DNA的纯度通过限制性内切酶消化、切口平移、引物延伸、用多核苷酸激酶进行末端标记和连接来证明。电透析成功用于完全去除抑制多核苷酸激酶反应的常见污染物以及从DNA样品中去除CsCl。

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