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Better binders. Fewer rounds. Six weeks to sequences.

Send us your antigen sequence. Designed candidates in 6 weeks, lab-validated binders in 9.

  • VHH · Fab · scFv · IgG · minibinder
  • You keep the IP
  • No immunisation, no animal

Discover your perfect antibody

Your project with us

Three ways to start with us

  • You have an antigen you need to target, with or without an epitope

    Let's design your antibody by de novo protein design, from your antigen sequence, with anticipated developability.

  • You have a reference sequence of your antibody

    We design your antibody around an existing sequence for higher diversity, developability, or for jumping to freedom to operate informed by prior art.

  • You already have antibody candidates

    Tell us about your candidates and your objective. Sequences are shared later, under a confidentiality agreement. We check developability, specificity, and improve yield and thermostability before you commit to scale-up.

  1. Kick-off + feasibility

    Days (free)

  2. Prototyping

    2 weeks

  3. Generative design & candidate selection

    3-4 weeks

  4. Wet-lab validation + QC

    up to 3 weeks

Engagement is progressive. You never commit to the next step before the previous one has been a success either for the generation, redesign or developability check.

See your project week by week

Supported capabilities

  • Antibodies

    Candidate binders against the exact site you want, from your antigen sequence alone.

  • Miniprotein binders

    Small, cheap-to-express binders for when an antibody scaffold is more than your target needs.

  • Antibody humanization

    Cut immunogenicity risk without paying for it in affinity.

  • Developability optimization

    Find the candidates that cannot survive development early, and re-engineer the ones that can.

  • Cross-reactivity

    Bind the species your preclinical package needs. Miss the paralogue that would sink it.

  • Affinity maturation

    Tighter binding designed on the interface itself, so you test tens of candidates instead of a library.

See it in action

  1. Designed against the exact site you need

    Six weeks to sequences against the site you named.

    Our technology
    • AntigenYour target
    • The epitope is specified, not random.
      • Aggregation designed out
      • Polyspecificity designed out
      • Glycosylation designed out
    We design the loops that grip your target.
  2. Rule out what can't work before the lab

    The risk can be read before anything is made.

    Case studies

    Developability profile

    Computed before synthesis

    • Sequence AInside the envelope on all five metrics
    • Sequence BOutside on CDR loop lengthNot disqualified: one to look at harder
    CDR loop lengthHydrophobic surfacePositive chargeNegative chargeVH–VL charge
    Two sequences from a natural repertoire, measured the same way as the 246 antibodies that reached the clinic. Shaded: the clinical envelope. Centre to edge: position among those 246.
  3. From your antigen to validated binders

    Nine weeks to binders validated in the laboratory.

    All services
    1. Your antigen

      Sequence or structure

    2. Your epitope

      Specified, not random

    3. De novo CDR design

      Loops that grip your target

    4. Developability filters

      Computed before synthesis

      • CDR loop length
      • Hydrophobic surface
      • Positive charge
      • Negative charge
      • VH–VL charge
    5. Ranked candidates

      Best ones to the wet lab

    Illustrated with PDB 1MEL.

The data behind EVOBodies™

Our sources

  • Clinical-stage antibodies
  • Natural antibody repertoire
  • Published developability metrics
  • Published structure predictors

What it rests on

  • 246antibodies that reached the clinic
  • 500natural antibodies, naive B cells of one healthy donor
  • 3independent structure predictors, so no single model decides
  • 6Bparameters in ESMC, the language model behind ESMFold2

5 developability metrics, measured the same way on both sets

What you get

Ranked sequences with the epitope each engages, and a developability profile per candidate.

Each number in your report is attributable, so your team can check it.

  • Private by design

    Your sequences and your target data serve your project, and nothing else.

  • Complete ownership

    You keep all rights to the antibodies we design for you.

  • 6 weeks

    From your antigen to designed sequences.

  • 9 weeks

    To wet-lab validation of the candidates.

Start designing better antibodies

We design developable antibodies using AI in under 6 weeks, wet-lab validated in 9 weeks, from your antigen sequence. No immunisation, no phage display, no animal.

Clients and partners

  • Diasource
  • Sagitta
  • CER Group
  • Livedrop
  • Synthelis
  • Twist
  • Welri
  • Cenaero LUCIA

Frequently asked questions

What is the expected timeline from our first conversation to delivery?

After our first discussion, we'll produce your free feasibility study in days, showing the confidence score for the next phases. Once you decide to move forward, you'll receive your designed antibody sequences after 6 weeks, wet-lab validated molecules from 9 weeks.

What starting material do I need to send you ?

Antigen sequence is enough.

How can I be confident this will work for my antigen ?

Every project starts with a free feasibility study, run before any commitment. We score your target from its 3D structure and tell you how much confidence we can have in generating antibodies against it. If that confidence is low, we say so plainly and we don't move forward, at no cost to you.

What is the background of IMMUNOCHEM?

Immunochem was founded in 1998 and spent its first two decades supplying high-quality research antibodies, with a speciality on small molecules. Since 2023, the company focuses on antibody discovery and generation by computational design, backed by wet-lab validation.

How to produce substantial amounts of antibodies in scale-up phase ?

Whatever the format (mAb, or single-domain antibody such as a nanobody or VHH), Immunochem delivers research-grade material and transfers the validated sequence and expression construct if appropriate. Gram-scale production runs with contract manufacturers.

Is the service available for my country?

The design work is computational and delivered digitally, so we serve customers worldwide from Belgium. Shipment of synthesised molecules follows standard research-reagent export rules, and no restriction applies in the European Union, the United Kingdom, Switzerland, the United States, India or China.