| Literature DB >> 8664153 |
S Günther1, J Herold, D Patzelt.
Abstract
A simple method is described for the extraction of high quality DNA for PCR amplification. The DNA was extracted by using Chelex-100 ion exchange resin or a special cell lysis buffer containing proteinase K. For further purification the DNA was bound to silica in the presence of a chaotrophic agent. Hence it is possible to unlimitedly wash the bound DNA and inhibitory substances are removed. By using diatoms as a source of silicates, this method is very economical and can therefore be used as a routine method.Entities:
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Year: 1995 PMID: 8664153 DOI: 10.1007/bf01844828
Source DB: PubMed Journal: Int J Legal Med ISSN: 0937-9827 Impact factor: 2.686