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. 2013 Aug 22;142(5):933–939. doi: 10.1017/S095026881300201X

Table 1.

Flu A(H3) and Flu A(H1) primers and thermal profile used in viral genome amplification

Detection method Gene Primer sequences 5′–3′ Location Thermal profile
Flu A(H3N2)
 PCR HA-1 H3-forward (H3f) 250–273 95°C for 10 min (×1)
CCTTGATGGAGAAAACTGCACAC 94°C for 45 s, 52°C for 30 s
H3-reverse (H3r) 567–588 72°C for 30 s (×40)
TGTTTGGCATAGTCACGTTCA 567–588 72°C for 5 min (×1)
Flu A(H1N1)
 PCR HA-1 H1- forward (H1f) 303–327 95°C for 5 min (×1)
GAATCATGGTCCTACATTGTAGAAA 95°C for 1 min, 55°C 1 min
H1-reverse (H1r) 1092–1117 72°C for 1 min (×25)
ATCDATTCCAGTCCATCCCCCTTCAAT 72°C for 7 min (×1)
Flu A/B multiplex real-time PCR
 FluA M GAGTCTTCTAACMGAGGTCGAAACGTA 13 FluAv_For
GGGCACGGTGAGCGTRAA 207 FluAv_Rev
FAM-TCCTGTCACCTCTGAC-MGB FluAv_TM
 FluB M TAGCAGAAGGCCATGAAAGCT 317 FluBv_For
CGTTCCTAGTTTTACTTGCATTGAAT 411 FluBv_Rev
JOE-TGTCTCATGGTCATGTACCT-MGBNFQ FluBv_TM