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. 2013 Feb 22;8(2):e57154. doi: 10.1371/journal.pone.0057154

Table 1. The primer sequences for microarray.

Primersa Sequence(5′-3′)f Location Targeted genesg Targeted viruses
NF1-1 CAAGAGTCTGAATGTGCATG 699–718c Neuraminidase 2009 influenza A (H1N1)
NF1-2 CAAGAGTCTGAATGTGTCTG 699–718c Neuraminidase Seasonal influenza A (H1N1)
NF1-3 CTGACCAACACCACCATA 221–238d Neuraminidase Influenza A (H3N2)
NR2-1b GGATCCCAAATCATCTCAAA 1131–1150c Neuraminidase 2009 influenza A (H1N1) Seasonal influenza A (H1N1)
NR2-2b CATCAATAGGGTCCGATA 482–499d Neuraminidase Influenza A (H3N2)
MF2-1 CGAATGGGGGTGCAGATGC 752–770e Matrix protein Seasonal influenza A (H1N1) Influenza A (H3N2)
MF2-2 CGAATGGGAGTGCAGATGC 752–770e Matrix protein 2009 influenza A (H1N1)
MR3-1b TCCACAGCATTCTGCTGTTCC 947–967e Matrix protein Seasonal influenza A (H1N1) Influenza A (H3N2)
MR3-2b TCCACAGCACTCTGCTGTTCC 947–967e Matrix protein 2009 influenza A (H1N1)
a

F for forward primers and R for reverse primers.

b

All the reverse primers with a Cy3- or biotin-labeled 5′-end.

c

Number of the position of the primer according to GenBank accession number CY081570.

d

Number of the position of the primer according to GenBank accession number CY091828.

e

Number of the position of the primer according to GenBank accession number HQ011421.

f

Nucleotides in italic showed the natural variants of different subtypes.

g

The primers for neuraminidase were used for oseltamivir-resistant mutation fragment amplification and the primers of matrix protein were used for amantadine-resistant mutation fragment amplification.