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. 2005 Mar;71(3):1546–1552. doi: 10.1128/AEM.71.3.1546-1552.2005

TABLE 4.

M. larici-populina primer pair specificity evauated by comparing Ct values in mixed DNA samples

Amt of M. medusae DNAa (ng) Amt of M. larici-populina DNAa (ng)
0 0.05 0.5 5
0 Noneb 21.4 ± 0.3 18.2 ± 0.8 14.3 ± 0.4
0.05 None 21.7 ± 0.4 18.1 ± 0.5 14.5 ± 0.7
0.5 None 21.2 ± 0.3 18.0 ± 0.4 14.4 ± 0.4
5 None 21.5 ± 0.4 18.1 ± 0.4 14.5 ± 0.5
Avgc None 21.4 ± 0.4 18.1 ± 0.5 14.4 ± 0.4
a

DNA was extracted from infected clone Jackii leaves at 10 days postinfection. The mixtures contained 0, 0.05, 0.5, or 5 ng of DNA isolated from M. medusae- or M. larici-populina-infected leaves. Amplification was carried out in triplicate with the M. larici-populina ITS primer pair.

b

None, no amplification detected.

c

Average for all 12 runs.