Recombinant human antibody to Env. 13.6A can neutralize HIV-1 isolates.
Figure 1 Neutralization profile of 205F Envs by autologous monoclonal antibody-containing supernatants from B cell hybridomas 13.6A.
Neutralization activity of 13.6A (B) B cell hybridoma supernatant was evaluated against pseudoviruses expressing autologous 205F Envs.
Rong, R., Li, B., Lynch, R. M., Haaland, R. E., Murphy, M. K., Mulenga, J., ... & Robinson, J. E. (2009). Escape from autologous neutralizing antibodies in acute/early subtype C HIV-1 infection requires multiple pathways. PLoS pathogens, 5(9).
Figure 2 Potential N-linked glycosylation sites in V1 and V2 modulate sensitivity to Mabs.
Neutralization of 0-month EnvPL6.3 and the sitedirected mutants shown in panel B was evaluated for 13.6A using reduction of luciferase production in JC53-BL13 cells.
Rong, R., Li, B., Lynch, R. M., Haaland, R. E., Murphy, M. K., Mulenga, J., ... & Robinson, J. E. (2009). Escape from autologous neutralizing antibodies in acute/early subtype C HIV-1 infection requires multiple pathways. PLoS pathogens, 5(9).
This is a product of Creative Biolabs' Hi-Affi™ recombinant antibody portfolio, which has several benefits including:
• Increased sensitivity
• Confirmed specificity
• High repeatability
• Excellent batch-to-batch consistency
• Sustainable supply
• Animal-free production
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