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. 2012 Dec 6;7(12):e50754. doi: 10.1371/journal.pone.0050754

Table 2. Cell-ELISA based cross-inhibition of PvTRAgs binding to erythrocytes by rabbit antibodies raised against the same antigen or against its close homolog.

Antigens Erythrocyte Binding Inhibition*
Self Antibody%±S.D. Homolog Antibody %±S.D
PvTRAg38 52.4±2.3 31±1.6 (PvATRAg74)
PvATRAg74 64.8±0.8 43.6±2.2 (PvTRAg38)
PvTRAg33.5 64.5±0.7 41.8±6.9 (PvTRAg35.2)
PvTRAg35.2 66.8±0.7 42.6±1.0 (PvTRAg33.5)
PvTRAg 52.9±2.6 34.2±0.6 (PvTRAg69.4)
PvTRAg69.4 63.5±0.3 42.9±5.6 (PvTRAg)
*

In a cell-ELISA assay, the Histidine tagged PvTRAgs were incubated with polyclonal antisera raised in rabbits at 1∶100 dilutions against the same antigen or its closest homolog (shown in brackets). Pre-incubated mixture was then allowed to react with erythrocytes and binding was detected by monoclonal anti-His6 antibody as described in the text. Binding of PvTRAgs in the absence of antibody is taken as100%. Values are mean ± standard deviation of three different experiments. The erythrocyte binding inhibition between self antibody and homologue antibody was significantly different (P<0.05).