Abstract
Current DNA extraction methods for parasites are labour-intensive and usually involve several steps, increasing the potential for cross-contamination. We describe here a closed-tube DNA extraction procedure based upon the use of a thermostable proteinase that enabled sensitive amplification of target loci from parasites from diverse lineages including Apicomplexa, Sarcomastgophora and Nematoda. Moreover, this procedure is not subject to cross-contamination and is readily adaptable to automation.
Original language | English |
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Pages (from-to) | 1831-1837 |
Number of pages | 7 |
Journal | Biotechnology Letters |
Volume | 29 |
Issue number | 12 |
DOIs | |
Publication status | Published - Dec 2007 |