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. 2013 Aug 2;11(8):2695–2712. doi: 10.3390/md11082695

Table 5.

Primers used for identification and screening of bacterial isolates.

Primer Sequence Tma ATb Reference
27fl AGAGTTTGATCCTGGCTCAG 61 55 [41]
1494rc TACGGCTACCTTGTTACGAC 59 55 [41]
DKF GTGCCGGTNCC(A/G)TGNG(T/C)(T/C)TC 67 55 [42]
DKR GCGATGGA(T/C)CCNCA(A/G)CA(A/G)(C/A)G 65 55 [42]
MTF2 GCNGG(C/T)GG(C/T)GCNTA(C/T)GTNCC 64 52 [43]
MTR2 CCNCG(A/G/T)AT(T/C)TTNAC(T/C)TG 47 52 [43]
ATfwd1 GT(A/C/G)TG(T/C)CC(A/T)(A/C)G(G/C)GA(T/C)GT(A/C/G)ATG 57 55 [44]
ATrev1 AT(A/G)TCCCA(A/T)(A/G)T(C/G/T)C(A/G)CA(A/G)TG 62 55 [44]

a Tm is the theoretical melting temperature of the PCR primers, given in °C; b AT is the annealing temperature used in PCRs containing these primers, given in °C.