Figure 3. Determining the recognition site of αRep9A8 on viral target protein CA₂₁-SP1-NC.

Indirect ELISA was used to investigate the interaction of αRep9A8 on immobilized synthetic peptides. Binding activities were reviewed by anti-His HPR and measured OD at 450 nm and the highest signal obtained from P9 was attributed the 1-unit value. y-axis; the relative biding activity, x-axis; list of peptides coated wells (P4–P12). Data shown represent the mean ± S.D. of the result in triplicates.