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Antibody Screening Capabilities

The right approach from the start, built for downstream success.

Display Screening
Single B Cell Screening
B Cell Sorting
Hybridoma
Functional Screening

Screening Strategy and Downstream Impact

Screening represents one of the most critical stages in antibody discovery, with direct implications for candidate quality and downstream development. Choosing the right approach, however, is not always straightforward. Factors such as target complexity, required data, and project timelines all need to be considered, along with the different aspects of antibody performance that each method captures.

Some approaches are designed to explore broad diversity and epitope coverage, while others enable more precise selection based on specificity or biological context. Nona offers a range of screening strategies to address these differences, helping ensure that candidates selected at this stage are aligned with downstream development.

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Exploring Broad Binding Diversity

Display technologies, including phage and yeast display, are designed to explore large antibody repertoires and identify binders across a wide range of epitopes. By constructing libraries from antibody sequences, these approaches enable screening at a scale that is not achievable with cell-based methods.

  • Library-scale diversity (10⁹–10¹⁰) enables identification of rare binders
  • Supports epitope-directed selection through controlled panning strategies
  • Yeast display enables affinity maturation and expression optimization

Display

Best suited for rapid identification of high-quality candidates from immunized repertoires where specificity, diversity, and confidence are critical

High-Resolution Selection from Immunized Repertoires

Single B cell screening using the Beacon platform enables direct evaluation of antibodies secreted from plasma cells, allowing candidates to be assessed in real time without the need for cloning or expression.

  • Screens antibody-secreting cells at the single-cell level, preserving native pairing and diversity
  • Enables sequential, multi-parameter assays on the same clone without enrichment steps
  • Provides early access to sequence, reducing bias from expansion and clonal dominance

Beacon Screening

Best suited for rapid identification of high-quality candidates from immunized repertoires where specificity, diversity, and confidence are critical

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Efficient Early-Stage Binder Identification

B cell sorting using flow cytometry enables direct selection of antigen-specific B cells based on surface-expressed antibodies, providing a straightforward approach for identifying binders from immunized repertoires.

  • Rapid identification of antigen-binding B cells using labeled targets
  • Maintains native immune-derived sequences without library construction
  • Compatible with both soluble and cell-surface antigens

B Cell Sorting

Best suited for early-stage binder identification when speed and simplicity are priorities

Established, Robust Antibody Discovery

Hybridoma technology remains a well-established approach for generating monoclonal antibodies from immunized animals, producing stable cell lines that continuously secrete antibodies for downstream evaluation.

  • Proven methodology with broad applicability across targets
  • Enables screening of secreted antibodies directly in supernatant, including functional assays
  • Generates stable clones for continued production and follow-up studies

Hybridoma

Best suited for programs requiring a robust, well-understood workflow or long-term antibody production

Selecting for True Functional Activity

CAR-based functional screening evaluates antibody candidates directly in a cellular context by expressing binders as CAR constructs, enabling selection based on biological activity rather than binding alone.

Best suited for rapid identification of high-quality candidates from immunized repertoires where specificity, diversity, and confidence are critical.

  • Screens antibody libraries in CAR format, linking binding to downstream signaling and activity
  • Identifies candidates based on functional outputs such as activation and cytotoxic response
  • Enables selection of high-performing binders that may not be identified through binding-based approaches
Learn More about Functional Screening

Choose the Right Screening Approach

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Explore Related Resources

AI-Enhanced Discovery Platform
Single B Cell Screening Platform
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