Products/Services Used | Details | Operation |
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Gene Synthesis> | Amplification reactions were conducted in final concentrations of genomic DNA at 1 to 3 ng µl–1, 200 µM dNTP (2.0 mM), 0.4 µM ITS6 and ITS4 primers, 1× Taq buffer (including 15 mM MgCl2), and Taq polymerase (GenScript Corporation, Piscataway, NJ) at 0.05 unit/µl. | Get A Quote |
Contemporary species identification relies strongly on sequence-based identification, yet resources for identification of many fungal and oomycete pathogens are rare. We developed two web-based, searchable databases for rapid identification of Phytophthora spp. based on sequencing of the internal transcribed spacer (ITS) or the cytochrome oxidase (cox) 1 and 2 spacer region, followed by BLAST searching the databases. Both databases are highly selective. For ITS, only sequences associated with published Phytophthora spp. descriptions or classic Phytophthora phylogenetics references are included. For the cox spacer region, only data obtained by resequencing select isolates reported in published work wer... More