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. 2010 Aug 11;48(10):3765–3769. doi: 10.1128/JCM.01069-10

TABLE 2.

Primers and adapters used in this study

Procedure and adapter/primer name Adapter/primer locationc Fragment no. Fragment size (bp) Nucleotide sequence (5′-3′)
Ligation-mediated PCR
    Eco1 NAd NA NA GAGTCGTGTTACTCCCATCG
    Eco2 NA NA NA AATTCGATGGGAGTAACACG
    ABg1a NA NA NA GAGTCGTGTTACTCCCATCG
    ABg2a NA NA NA GATCGATGGGAGTAACACGACTC
    IS1b IS711 NA NA CGGTTCCATTGCTCATCTGT
Fragment-specific PCR
    I1 BR1657 I 253 CTACATAGGCATCGCCAGAG
    II1 BRA0655 II 750 TGCCATAGGGCACATTGTTC
    III1 BR1612 III 523 TTATATGATGCGCCCGGAGG
    IV1 BR0613 IV 670 GAAGGTAGAGCCGGAATATC
    V1 BR0625 V 195 GCTTTCGCATTGGAGCTTAC
    IS2 IS711 I through V NA GCTCACGGCTGTTCTCCTTT
a

The same adapters and primers were used for LM-PCR with restriction enzymes BglII and BamHI.

b

All LM-PCRs were performed with primer IS1.

c

According to the genome sequence of B. suis 1330 chromosome I or II.

d

NA, not applicable.