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. 2007 Mar 9;73(9):2911–2918. doi: 10.1128/AEM.02176-06

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Copyright © 2007, American Society for Microbiology

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FIG. 1. — PCR amplifications using primers Pm1 and Pm2 on DNA extracts from Phaeoacremonium (lanes 1 to 9) and other fungal species (lanes 10 to 15). Lanes: M, molecular size markers (100 bp); 1, P. aleophilum (CBS 246.91); 2, P. parasiticum (CBS860.73); 3, P. inflatipes (CBS391.71); 4, P. mortoniae (CBS101585); 5, P. angustius (CBS114992); 6, P. viticola (CBS101738); 7, P. scolyti (CBS113597); 8, P. krajdenii (CBS 109479); 9, P. venezuelense (CBS651.85); 10, Botryosphaeria parva; 11, Phomopsis spp.; 12, Phaeomoniella chlamydospora; 13, Botryosphaeria obusa; 14, Phialophora mustea; 15, Phialemonium dimorphosporum; 16, grapevine DNA; 17, no DNA.