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. 2017 Jul 24;17:164. doi: 10.1186/s12866-017-1080-9

Table 2.

List of primers and probes

Name Fluorochrome Sequence (5’➔ 3′) Quencher Nt Tm (°C) Degeneracy
F1 GGTGCGATGATGAAGTCTGG 20 60.5 0
R1 CTATGATATTGACTTCCATGTTCA 24 58.3 0
F2A ATGATGAARTCIGGIATGTTYYT 23 53.9–59.2 8
F2B ATGATGAARTCNGGNATGTT 20 50.2–56.4 32
R2A ATYTTIACTTCCATGTTCATCCA 23 55.5–57.6 2
R3A ATYTTIACTTCCATRTTCARCCA 23 53.9–59.2 8
R4A ATYTTIACTTCCATGTTGACCCA 23 57.6–59.2 2
R2B ATYTTNACTTCCATGTTCATCCA 23 55.5–59.2 8
R3B ATYTTNACTTCCATRTTCARCCA 23 53.9–60.9 32
R4B ATYTTNACTTCCATGTTGACCCA 23 57.6–60.9 8
P1 ATTO425 AT + GTT + GTC + GT + CN + CC BHQ1/LNA™ 14 40.8–43.7/66–69 4
P2 ATTO425 AT + GTT + GTC + GT + CIC + CIAT BHQ1/LNA™ 17 47.5/67 0

Variable melting temperature was indicated for degenerate primers. Degenerate nucleotides were shown in bold. Y accounted for C/T, R for A/G, N for A or T or C or G. I was used as an alternative for N. ATTO425 labeled probes were quenched using Black Hole Quencher 1 (BHQ1). Locked Nucleic Acid nucleotides (LNA™) were prefixed with a “+” sign and the resulted increase in Tm was indicated following use of Exiqon™ tool for calculation