ICDMO's antibody development platform integrates immunology expertise, advanced hybridoma technology, phage display, and recombinant expression to deliver custom antibodies of exceptional quality. Whether your goal is a research-grade polyclonal serum, a hybridoma-derived monoclonal for diagnostic standardization, or a sequence-defined recombinant IgG for therapeutic development, our team manages every step from antigen design through application validation.
Every antibody project is supported by rigorous titer monitoring, specificity confirmation, and application-specific validation. We offer optional epitope mapping, affinity measurement (SPR/BLI), isotype determination, and conjugation services to deliver a fully characterized antibody ready for your intended use.
Each platform is supported by dedicated scientists with deep immunology and protein engineering expertise.
Note: All timelines are estimates for standard projects. Complex antigens or low-immunogenicity targets may require additional immunization rounds. For GMP-grade therapeutic antibody production, please contact us for a customized development plan.
Antibody scientists respond within 24 hours with a tailored development plan and pricing.
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