We develop antibodies targeting the heavily glycosylated HIV-1 envelope protein, enabling research into viral entry, neutralization, and vaccine design.
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Viral surface glycans form dense shields that regulate host-cell entry and protect critical epitopes, complicating immune recognition. Studies on HIV, influenza, coronaviruses, and flaviviruses show that glycan positioning can determine neutralization breadth, escape potential, and vaccine success. Targeting glycan-dependent viral epitopes with precise antibodies is emerging as a powerful approach for diagnostics, therapeutics, and immunology research.
Are you facing challenges with viral immune evasion, difficulty in isolating glycan-dependent epitopes, or poor cross-reactivity control in antibody development? Anti-viral glycan antibody development services at Creative Biolabs help you generate high-specificity, functional antibodies through advanced glycoengineering, immunogen design, and comprehensive validation platforms.
To ensure the successful development of anti-viral glycan antibodies, we apply a range of well-defined strategies that integrate precision design, advanced platforms, and rigorous validation.
We prepare chemoenzymatically synthesized viral glycans—including high-mannose, hybrid, and complex structures—to recreate authentic viral surfaces.
Our experts design glycoengineered immunogens that expose conserved viral epitopes while masking variable regions, enabling broad neutralization potential.
We deploy glycan arrays and competitive binding panels to eliminate off-target interactions with host-like glycans, ensuring antibody safety and accuracy.
Every candidate is evaluated using receptor-binding inhibition, lectin competition, and neutralization assays to confirm functional impact.
Advanced glycoproteomics and molecular modeling reveal glycan shifts across viral variants, guiding antibody design and risk assessment.
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Monoclonal, humanized, or fully human antibodies tailored to glycan-dependent viral epitopes, suitable for therapeutic, diagnostic, or research applications.
Production of glycopeptides and glycoconjugates with native-like structures for immunization or screening platforms.
Testing across glycan microarrays, SPR/BLI, ELISA, and cell-based assays to confirm accuracy in the desired application.
Comprehensive deliverables including specificity, kinetics, epitope mapping, and cross-reactivity data for seamless integration into client workflows.
We develop antibodies targeting the heavily glycosylated HIV-1 envelope protein, enabling research into viral entry, neutralization, and vaccine design.
Custom antibodies against SARS coronavirus spike glycoproteins, supporting studies of receptor binding, immune evasion, and therapeutic interventions.
Antibody generation against Ebola GP to advance diagnostics, neutralization assays, and therapeutic research for hemorrhagic fever.
We design antibodies for the Tomato spotted wilt virus G1 glycoprotein, aiding plant pathology research and diagnostic development.
Production of antibodies targeting the rabies virus glycoprotein G, supporting vaccine research and viral pathogenesis studies.
Custom antibodies for influenza hemagglutinin and neuraminidase glycoproteins, facilitating vaccine, therapeutic, and epidemiological research.
Antibody development against hepatitis C virus glycoproteins E1/E2 for neutralization studies, diagnostics, and therapeutic applications.
Generation of antibodies targeting HBV surface glycoproteins, enabling improved diagnostic assays and therapeutic exploration.
We provide antibodies against rotavirus glycoproteins for vaccine development, diagnostic tests, and virology research.
Development of antibodies against Lassa virus glycoprotein complex to support diagnostic and therapeutic research for arenavirus infections.
Production of antibodies targeting dengue virus envelope glycoproteins to aid neutralization studies, diagnostics, and vaccine research.
Custom antibodies against Zika virus glycoproteins, supporting detection, neutralization, and immunological investigations.
We generate antibodies against the Nipah virus fusion protein to facilitate pathogenesis studies and therapeutic design.
Antibody development targeting Hendra virus glycoproteins, enabling research into zoonotic infection and countermeasure development.
Antibodies against EBV glycoproteins to support diagnostic assay development and studies of viral latency and oncogenesis.
Generation of antibodies to JEV glycoproteins for use in diagnostics, vaccine improvement, and viral pathogenesis research.
Custom antibodies for Hantaan virus glycoproteins to aid in immunological studies, diagnostics, and therapeutic research.
Development of antibodies targeting WNV glycoproteins, supporting surveillance, vaccine studies, and therapeutic development.
Production of antibodies against Newcastle disease virus glycoproteins for poultry vaccine development and virology research.
Generate authentic or engineered glycans and glycoproteins, verified by MS/HPLC for structural fidelity.
Apply hybridoma or phage display platforms, guided by immunofocusing strategies, to enrich for conserved glycan-dependent epitopes.
Perform glycan-array testing, ELISA, and SPR/BLI to confirm epitope-specific binding and eliminate off-targets.
Assess receptor-blocking, lectin inhibition, neutralization (pseudo/live virus), and Fc-effector assays for mechanistic validation.
Improve lead candidates with affinity maturation, isotype selection, or Fc-engineering to meet performance goals.
Deliver datasets including specificity, binding kinetics, stability, and cross-reactivity, ready for scale-up or diagnostic use.



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Glycosylation across the SARS-CoV-2 spike protein trimer forms a dense array of N-linked glycans that functions as a protective shield, covering large regions of the protein surface and masking critical epitopes from immune surveillance. This glycan layer reduces accessibility of neutralizing antibody binding sites, thereby complicating the natural immune response and antibody-based therapeutic development. At the same time, selective gaps within the glycan shield expose conserved domains that can be targeted for antibody recognition. Understanding the balance between shielding and accessibility provides valuable insight for designing vaccines and monoclonal antibodies with improved efficacy, as it highlights how structural glycan arrangements influence both viral infectivity and antibody generation.
Fig.1 The protective role of glycan coverage on the spike protein trimer.1
High-specificity Reagents
“Using Creative Biolabs’ anti-viral glycan antibody development services in our research has significantly improved our ability to detect glycan-dependent viral epitopes with minimal cross-reactivity.” [Dr. T***]
Reliable Neutralization
“Using Creative Biolabs’ anti-viral glycan antibody development Services in our research has significantly facilitated the identification of broadly neutralizing antibodies against influenza glycoproteins.” [Dr. M***]
We develop antibodies for viruses such as HIV, influenza, coronaviruses, HCV, and ZIKV, where glycans are critical for infection and immune evasion.
Cross-reactivity is minimized through glycan-array panels and competitive assays with host-like glycans before candidate advancement.
We perform glycoconjugation by linking glycans to proteins, peptides, or nanoparticles, enhancing immunogenicity and enabling applications in vaccines, diagnostics, and glycan research. Conjugates are customized for stability and reliable assay performance.
We deliver solutions for glyco-based vaccine design, using defined glycans and engineered immunogens to trigger targeted immune responses. This service supports infectious disease and cancer vaccine development by focusing on glycan epitopes that drive effective immunity.
Creative Biolabs’ Anti-viral glycan antibody development services integrate immunogen authenticity, stringent validation, and translational focus, providing clients with reliable tools to tackle viral immune evasion and advance discovery. Contact Creative Biolabs to unlock the potential of viral glycan biology.
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