Recombinant Mouse Antibody (1AF10) is capable of binding to TGEV S protein, expressed in Chinese Hamster Ovary cells (CHO). Antibody binding to RBD mutants showed that site A epitopes extend across the TGEV RBD tip, although there are some differences among the three A subsites. The epitopes recognized by Aa- and Ab-specific mAbs bear the exposed TGEV Trp571 residue at the β3–β4 loop, whereas epitopes for the Ac-specific mAbs center on Tyr528 in the β1–β2 turn.
Figure 1 APN-binding domain and epitopes for neutralizing mAbs overlap in TGEV and PRCV S proteins.
C. Binding of site A-specific TGEV-neutralizing mAb to the SA protein. mAb binding to plastic-bound SA protein, monitored by optical density (OD). Site A mAbs are specific for the Aa (1BB1), Ab (1DE7) and Ac (6AC3, 1AF10) subsites [24]. An anti-HA mAb that binds to the HA tag in the SA protein was used as control. D. Site A-specific mAbs prevent SA protein binding to pAPN. Binding of the SA protein to BHK-pAPN cells in panel B was monitored alone or in the presence of site A (shown in C) or site D-specific (1DG3) mAb, and the binding ratio determined. C, D. Mean and standard deviation for three experiments.
Reguera, J., Santiago, C., Mudgal, G., Ordoño, D., Enjuanes, L., & Casasnovas, J. M. (2012). Structural bases of coronavirus attachment to host aminopeptidase N and its inhibition by neutralizing antibodies. PLoS pathogens, 8(8), e1002859.
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• Increased sensitivity
• Confirmed specificity
• High repeatability
• Excellent batch-to-batch consistency
• Sustainable supply
• Animal-free production
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CAT | Product Name | Application | Type |
---|---|---|---|
PABZ-139 | Recombinant Human Anti-SARS S Antibody (80R) | Neut | IgG |
PABL-719 | Recombinant Mouse Anti-TGEV Spike protein Antibody (1AF10) | ELISA, Neut | IgG |
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