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. 2012 Feb;80(2):832–838. doi: 10.1128/IAI.05681-11

Table 1.

Peptide fragments used in epitope-mapping experiments and reactivity of the MAbsa

Fragment (aa start-end) Primer (5′-3′ sequence)
EIA titerb
Forward Reverse MAb 2B11 MAb 1E11
N1 (31-372) N1for (CACCAAAGATGCAATGGAAAGAAC) Bflrev (TTATGCTTTTTTCGTATCTACTTTAATAT) 640 >640
N2 (61-372) N2for (CACCAATGTATCGTCTGTTGATG) Bflrev (TTATGCTTTTTTCGTATCTACTTTAATAT) 320 >640
N3 (93-372) N3for (CACCCCACAGCTTATTTCAACG) Bflrev (TTATGCTTTTTTCGTATCTACTTTAATAT) 320 >640
N4 (122-372) N4for (CACCGCAAAGGATAAAGCAACT) Bflrev (TTATGCTTTTTTCGTATCTACTTTAATAT) 160 >640
N5 (152-372) N5for (CACCGACCTGAAGAAATTCCG) Bflrev (TTATGCTTTTTTCGTATCTACTTTAATAT) >640
C1 (205-258) C1for (CACCATTATTATCGGTTCATC) C1rev (CTTGCGTAATACGATTCCAG)
C2 (251-324) C2for (CACCACAGCTGGAATCGTATTA) C2rev (AAGTAAAGAATTGTATTTTGATCC)
C3 (314-372) C3for (CACCTACACAATGGGATCA) C3rev (TGCTTTTTTCGTATCTACTAC) >640
a

Amino acid (aa) numbering according to Granum et al. (14), without signal peptide. Gray shading in the forward primer sequences indicates additional nucleotides needed for directional cloning approach.

b

Reciprocal dilution. –, Negative at the lowest dilution tested (1:5).