Plant Science Unit, USDA-ARS, 1605 Albrecht Boulevard, Fargo, ND 58105-5674, USA, Small Grains Research, USDA-ARS, 1605 Albrecht Boulevard, Fargo, ND 58105-5674, USA.
Mol Ecol Resour. 2008 Jan;8(1):83-7. doi: 10.1111/j.1471-8286.2007.01907.x.
A fast, efficient technique is described for the extraction of DNA from a large number of samples. The applications of this method include population genetics, plant breeding, and genetic screening. In the field, samples are collected in premeasured silica gel aliquots in polypropylene blocks, which are later used to grind the dried tissue. This permits naturalists, breeders, and collaborators to collect a large number of samples in a short amount of time and allows the samples to dry quickly during shipping. No phenol or chloroform steps are required to obtain high-quality DNA. Samples representing 12 plant families, three invertebrates, and a mammal were included. Quantities of DNA obtained were consistent with or better than other techniques. The quality of samples was tested by amplification of the internal transcribed spacer region. Test amplifications were successful, confirming the quality of extracted DNA.
一种快速、高效的从大量样本中提取 DNA 的技术。该方法的应用包括群体遗传学、植物育种和遗传筛选。在野外,将样本收集在聚丙烯块中的预先测量的硅胶等分试样中,然后用于研磨干燥的组织。这使得自然学家、育种者和合作者能够在短时间内收集大量样本,并允许样本在运输过程中快速干燥。不需要苯酚或氯仿步骤即可获得高质量的 DNA。实验中包括了 12 个植物科、3 种无脊椎动物和 1 种哺乳动物。获得的 DNA 量与其他技术一致或更好。通过扩增内转录间隔区测试了样本的质量。测试扩增成功,证实了提取 DNA 的质量。