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. 2013 Apr 25;4:107. doi: 10.3389/fmicb.2013.00107

Table 2.

Primers and PCR conditions for MLSA.

Genes Primer name Primers (5′−3′) Primer combination and annealing temperature (°C) Amplicon size (bp)
atpA atpA101F ADGTDGGWGAYGGTGTYGC 101F-1081R: 55 980
atpA1081R CGTTRATAGCWGGTCTDATACC
atpA983R ACGTCACCBGCYTKWGTTTC 101F-983R: 52 882
dnaK dnaK464F GDCARGCWACMAARGAYGC 55 741
dnaK1118R GCMACWACYTCRTCDGG
gyrB gyrB377F CTYCAYGGWGTWGGWGC 52 1186
gyrB1563R TCWACRTCRGCRTCHGYCAT
napA napA181F TTCTGTGGWACDGGWTGYGG 181F-1713R: 59 1532
napA690F* ATGGCWGARATGCAYCC
napA1714R CKBGCHGCTTTRATCCARTG
napA1347R* GRTTVAWWCCATTGTCCA
metG metG145F ACRGGWACMGATGARCATGG 55 686
metG831R GCDGGCCARTAWACDGYATG
tkt tkt478F AWSGSYGTRGGTATGGC 52 1063
tkt1541R TGKGTWGGDCCRTCYTC
*

Primers used for sequencing reaction.