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. 2023 Mar 22;14:1161287. doi: 10.3389/fmicb.2023.1161287

Table 2.

Primers used for Bovine ephemeral fever virus (BEFV) genome amplification in this study.

Primer pairs Sequence (5′–3′) Locationsa Length of amplicon (bp)
1 ACGAGAAAAAACAAAAAAACTAATTGATA 1–29 2,728
GCAGTTCCGGTGAATTCTATTACCTCG 2,702–2,728
2 TTCAAAACCAATAGAAAGAACAAC 2,522–2,545 1,698
TAAGATCCGATCCCATAATGAT 4,198–4,219
3 ACAGATAGAACAGAATTTGAAG 3,921–3,942 1754
GCTTAATCAACTCTAGTCTAAT 5,653–5,674
4 ATTATCCTCCTCCAAAGTGCGA 5,393–5,414 1,560
TCAATATAATCCAAAATCCTAG 6,931–6,952
5 AACAGGCAATGGAGAAAGG 6,815–6,833 2,368
GTTTGAAACCTGCTAATTA 9,164–9,182
6 GGACATAAGTGGACGGTGGATA 9,063–9,084 1967
TTTCTCCTCTGATTGCTGGATT 11,008–11,029
7 GGAACAATAAAGGGACTGCCAA 10,807–10,828 2018
GTGAACTCTGATATAAATGATG 12,803–12,824
8 GGTAGGTGATTCACTGTTAAGT 12,582–12,603 1,375
AGCATGTCTAATATATTTGTA 13,935–13,956
9 GAAACAGAATTCTATGATGATTGACCTGAT 13,767–13,788 1,133
ACGAAGAAAAACAAATAAAATACAATTCCT 14,870–14,899
a

The location is determined based on the representative strain Bovine/China/Henan1/2012 (KM276084.1).