Additional file 8.

Primers used for PCR amplification/sequencing of ITS2 in the nuclear-encoded rRNA operon of the Ulvales. Since a few cultures were contaminated with fungi, PCR reactions were performed with specific reverse primers that mismatched with fungal rDNA sequences (labelled 'exFungi'; specific 3'-positions underlined).

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Caisová et al. BMC Evolutionary Biology 2011 11:262   doi:10.1186/1471-2148-11-262