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Bispecific Antibody Production and Development Services

Bispecific Antibody Production Services

Bispecific Antibody Development From Design to Scale-Up

From IgG-like to fragment-based formats, we design and produce the bispecific antibody format that fits your target, application and development stage.

  • 40+ bispecific formats
  • IP-conscious formats
  • 4–6 weeks production

Discuss your projectTalk to our experts

Start from existing antibody sequences or involve our team earlier for discovery and engineering.

Bispecific antibody formats

Bispecific Antibody Production Services for
Every Format

With expertise spanning IgG-like and fragment-based, symmetric and asymmetric bispecific antibody formats, we help select and produce the format best suited to your target, application, performance requirements and budget.

  • BiTE

  • Diabody

  • DART

  • DVD-Ig

  • IgG(H)-scFv

  • scFv-(L)IgG

  • HSAbody

  • Fab-scFv

  • IgG-IgG

  • F(ab’)2

  • + More

40+ bispecific formats

Looking for another format? Discuss your project with our experts.

Discuss Your Format

Multiple Pairing Strategies for Correctly Assembled Bispecifics

Correct chain pairing is the central engineering challenge of any IgG-like bispecific. We combine the right techniques depending on your project and format of choice.

  • Knob-into-Hole (KIH)

    Promotes correct heavy-chain heterodimerization.

    Solves: heavy chain / heavy chain mispairing

  • CrossMab

    Domain crossover guides correct light-chain association.

    Solves: light chain / heavy chain mispairing

  • Kλ-body

    Uses kappa and lambda light chains to support correct pairing.

    Solves: light chain / heavy chain mispairing (via downstream separation, not steric design)

  • Duobody

    Controlled Fab-arm exchange generates bispecific IgG molecules.

    Solves: heavy chain pairing, without co-expression

  • Dock and Lock

    Uses complementary dimerization and anchoring domains.

    Solves: multi-domain assembly beyond simple 1+1 bispecifics

Bispecific antibody development

From Sequence to a Validated Bispecific Candidate in 4–6 Weeks

Developing a bispecific antibody is often complex: format choice can influence binding behavior, stability, half-life, manufacturability and therapeutic potential. We help you compare relevant formats and make data-driven go/no-go decisions before scale-up.

Discuss your bispecific development project

Bispecific antibody production

Custom Production From mg to Gram Scale

Bispecific antibodies are expressed using the high-performance proprietary XtenCHO™ Race platform. Antibody gene sequences are optimized specifically for this system to ensure high yields and low endotoxin levels.

  • mg → grams
    production scale

  • Up to 98%
    purity

  • 1 g/L
    yield in stable cell line

  • <0.1 EU/mL
    endotoxin upon request

Tell Us About Your Bispecific Antibody Project

Already have antibody sequences or need support earlier in development? Tell us where your project stands and our team can help define the next step.

  • Bispecific format selection
    Select and compare formats according to your project requirements.
  • Bispecific antibody production — 
    Move from selected sequences to production and characterization.
  • Stable cell line development
    For projects moving toward larger-scale, reproducible production.
  • Antibody discovery — 
    If you don’t yet have suitable parental antibodies.

Not sure which service or format you need?

Send us your project requirements and our team can help you identify the most appropriate approach.

Scale-up

Scale Your Bispecific Antibody Production

Move from early-stage production to larger, reproducible supply through stable cell line development.

  • XtenCHO™ Race
    Proprietary cell line

  • Stable cell line development
    Gram-level and larger-scale production

  • Customizable endotoxin level
    According to project requirements

Discuss Your Scale-Up Project

Learn More About Stable Cell Line Development

Intellectual property

Fully IP-Free, From Sequence to Cell Line

The sequences, the antibody, and the cell line stay yours, with no shared IP and no royalties down the line from ProteoGenix.

  • No IP constraints or royalties from ProteoGenix
  • Our experts can help you avoid mutations patented by others

Contact Our Experts Book a Call

Case Report bispecific antibodies

Case report

Engineering Seven Bispecific Antibody Formats Yielding Nanomolar Leads Against Prostate Cancer

A Swedish biotech company trusted ProteoGenix with the design and production of multiple bispecific antibody formats. The customer supplied sequences from two monoclonal antibodies, Ab1 and Ab2, which served as the foundation for bispecific engineering.

  • 7 bispecific formats designed
  • 3.20 × 10⁻¹⁰ M affinity of the best candidate

Read the case report

Expert guidance

Inside ProteoGenix: Navigating Bispecific Complexity

Anne shares her experience guiding a client through a bispecific antibody project — from early design questions to the format decisions that made the difference.

Inside Proteogenix navigating bispecific complexity

Scientific track record

Clients’ Publications Powered by ProteoGenix’s Expertise

Selected scientific publications involving bispecific antibody research and development.

Publications
mAbs

Danquah, W., Pichery, M., Eden, T., Boyance, A., Pasquet, L., Roure, V., Mars, M., Marchand, A., Gumz, E., Gador, M., Valente, L., Contini, M., Czernecki, L., Shanmuganathan, S., Barron, P., Chabot, S., Dangl, M., & Niederfellner, G. (2026). Combination therapy with a novel CD2-targeted costimulatory bispecific antibody overcomes limitations of CD3 T cell engager treatment for solid tumors. mAbs, 18(1), Article 2684378.

View publication

Publications
Journal of Biological Chemistry

De Nardis, C., Hendriks, L. J. A., Poirier, E., Arvinte, T., Gros, P., Bakker, A. B. H., & de Kruif, J. (2017). A new approach for generating bispecific antibodies based on a common light-chain format and the stable architecture of human immunoglobulin G1. Journal of Biological Chemistry, 292(35), 14706–14717.

View publication

Publications
The AAPS Journal

Liu, W., Yang, J., Yan, W., & Peng, K. (2025). Reformation of a clinical anti-drug antibody assay to enable the immunogenicity assessment of a bispecific antibody biotherapeutic. The AAPS Journal, 27(1), Article 12.
View publication

Publications
Blood

Bray, J. S., Thomas, G. R., Smith, V. M., Jayne, S., Dyer, M. J. S., & Walter, H. S. (2024). Comparative in-vitro efficacy of CD20xCD3 IgG bispecific biosimilar constructs against diffuse large B cell lymphoma (DLBCL) cell lines with different levels of expression of CD20. Blood, 144(Supplement 1), Article 5826. 
View publication

Publications
British Journal of Haematology

Bray, J. S., Thomas, G. R., Smith, V. M., Wright, A., Jayne, S., Dyer, M. J. S., & Walter, H. S. (2025). In vitro comparison of CD20xCD3 bispecific antibodies against diffuse large B-cell lymphoma (DLBCL) cell lines with different levels of expression of CD20. British Journal of Haematology, 206(5), 1350–1354. 
View publication

Publications
Applied Biochemistry and Biotechnology

Sandeep, Shinde, S. H., Ahmed, S., Sharma, S. S., & Pande, A. H. (2026). Engineering and partial characterization of an anti-IL-23/anti-TNF-α bispecific domain antibody fused to human serum albumin domain for inflammatory disease therapy. Applied Biochemistry and Biotechnology, 198(7), 5212–5230. 
View publication

Interactive tool

Is Your Bispecific Antibody Ready for the Next Step?

Use the checklist prepared by our experts to assess antibody readiness across general and specialized bispecific criteria.

Download the checklist

Frequently Asked Questions

Need a quote or advice on
your bispecific antibody?

Tell us where your program stands — existing sequences, format selection, pilot production, characterization or scale-up — and our team can recommend the most relevant next step.

  • Dedicated project guidance
  • Format selection adapted to your target and constraints
  • Production and QC from early screening to scale-up

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