Hansen J C, Rickett H
Department of Biochemistry and Biophysics, Oregon State University, Corvalis 97331.
Anal Biochem. 1989 May 15;179(1):167-70. doi: 10.1016/0003-2697(89)90219-4.
Linear double-stranded DNA fragments ranging from 0.14 to 8.4 kbp have been fractionated on low-percentage agarose exclusion gels. Both Ultragel A2 (2% agarose) and Bio-Gel A150m (1% agarose) exclude DNA fragments greater than 900 bp, while the exclusion limit of Bio-Gel A50m (2% agarose) is about 350 bp. All gels result in moderate resolution of DNA fragments smaller than the exclusion limits; we generally observe nearly complete one-step separation of fragments that differ in size by a factor of 2. On the basis of these results, we have used these exclusion gels to routinely purify greater than 0.4 mg of plasmid insert DNA sequences in one step and over 2.5 mg with a single column, demonstrating that these gel matrices can be ideally suited for repeated rapid large-scale purification of plasmid inserts. In addition, this knowledge allows for a more rational design of plasmids in those cases where large-scale use of the insert DNA is required.
长度在0.14至8.4千碱基对之间的线性双链DNA片段已在低百分比琼脂糖排阻凝胶上进行了分级分离。Ultragel A2(2%琼脂糖)和Bio-Gel A150m(1%琼脂糖)均可排阻大于900碱基对的DNA片段,而Bio-Gel A50m(2%琼脂糖)的排阻极限约为350碱基对。对于小于排阻极限的DNA片段,所有凝胶都能实现适度的分辨率;我们通常观察到,大小相差2倍的片段几乎能一步完全分离。基于这些结果,我们已使用这些排阻凝胶常规地一步纯化超过0.4毫克的质粒插入DNA序列,单柱可纯化超过2.5毫克,这表明这些凝胶基质非常适合重复快速大规模纯化质粒插入片段。此外,在需要大规模使用插入DNA的情况下,这一知识有助于更合理地设计质粒。