Binder Discovery
Fast identification of sequence-verified scFv and VHH binders
Human scFv and VHH discovery powered by yeast display screening, quantitative flow cytometry, and iterative enrichment workflows.
Best for teams that need a practical binder panel quickly to support screening, validation, or go/no-go decisions.
Which format should I choose?
- Choose scFv for human-compatible discovery and standard antibody development paths.
- Choose VHH for compact binders and access to challenging or recessed epitopes.
- Run both in parallel when epitope diversity or backup coverage is critical.
Best Fit Scenarios
- Fast-follow programs requiring rapid binder generation.
- Multiple binders needed for screening, validation, or backup.
- Benchmark antibody, ligand, or competitor binder available.
- Difficult, conserved, small-protein, or membrane-associated targets.
- Early programs needing quick go/no-go data before larger investment.
Inputs
- Purified protein, Fc-fusion, bead-coupled target, peptide, or cell-surface target.
- Biotin / streptavidin systems, direct fluor labeling, secondary detection, or custom assay formats.
- Program goals such as blocking, internalization, epitope diversity, affinity tier, or species cross-reactivity.
Deliverables
- Sequence-verified binder panel ready for downstream evaluation.
- Ranked clone set with clear prioritization.
- Round-by-round enrichment summary.
- Screening-level binding curves and titration profiles.
- Screening-level affinity tiering to support clone selection.
- Recommendations for IgG, Fc, soluble VHH, or follow-up development.
Data Confidence
- Quantitative flow cytometry-based screening.
- Round-by-round enrichment tracking.
- Internal controls to monitor specificity, background, and reagent binding.
- Reproducible selection workflows designed for practical decision-making.
