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. 2008 Mar 19;149(2):264–268. doi: 10.1016/j.jviromet.2008.01.023

Table 2.

Details of PCR and LAMP primers designed for detection of capsid protein coding sequences of PCV2

Primer namea Genome position Squence
F 596–617 5′-ATGGGCTGCTAATTTTGCAGAC-3′
B 961–982 5′-TCAATAGGAAATTCAGGGCATG-3′



FIP 762–783 5′-GTACAGTTCCACCTTTAGTCTC+TTTT+
659–680 GGTTACCATGGTGAAGAAGTGG-3′



BIP 840–861 5′-CAACTGCTGTCCCAGCTGTAGA+TTTT+
910–931 TCCTCCGTGGATTGTTCTGTAG-3′
a

The primers of F, B, FIP and BIP were for LAMP and each inner primer of LAMP has two binding regions connected by a TTTT spacer. Primers of F and B were also applied in PCR.