Skip to main content

It looks like you are visiting from outside the EU. Switch to the US version to see local pricing in USD and local shipping.

Switch to US ($)
Phage display services

Phage display services –
3 guaranteed binders in 2 weeks

With 25+ years of experience and a track-record of more than 500 phage display projects, ProteoGenix can confidently guide you to your project’s success and offer the strongest guarantees of the market.

  • 12 proprietary phage display libraries: naive & immune
  • World’s first human cancer & autoimmune libraries
  • Fully IP-freeno royaltiesno milestone payment

Talk to our expertsExplore our libraries

Why ProteoGenix

A phage display platform designed for challenging targets

Discover why more than 9,000 researchers choose ProteoGenix.

  • Guaranteed Results

    3 binders guaranteed

    If fewer than three qualified binders are identified, we screen 96 additional clones at no extra cost.

  • Library diversity

    5 species including human

    Access human, rabbit, camelid, dog and cat phage display libraries selected for your project.

  • Proprietary Libraries

    12 libraries

    Immune, naïve and disease-specific libraries, including human cancer and autoimmune repertoires.

  • Fully Custom

    Application-specific strategies

    Library choice, panning and screening are adapted to your antigen and success criteria.

  • No hidden fees

    Full IP Ownership

    No royalties, milestone fees or licensing restrictions. The agreed sequences belong entirely to you.

  • Scientific guidance

    Dedicated PhD expert

    Your dedicate PhD Expert will guide you and provide advice throughout your entire project 

Proprietary screening resources

ProteoGenix phage display library portfolio

Screen against 12 proprietary immune and naïve libraries covering human (including unique cancer and autoimmune repertoires), camelid (VHH), rabbit, dog, and cat species, alongside robust peptide libraries. Together, this portfolio offers more than 200 billion clones with a guaranteed in-frame rate of at least 93%—engineered to deliver high-affinity hits, fast.

  • 12
    proprietary libraries

  • 5
    species represented

  • >200B
    combined clones

  • ≥93%
    in-frame sequences

Immune Libraries for Immediate High-Affinity Hits

Get high-affinity binders immediately designed for your application. Immune libraries allow strong hit rate with fewer panning rounds.

Library Species Format Donor Diversity
LiAb-SFCOVID-19™ Human scFv Donors who recovered from COVID-19 1.19 x 10¹⁰ clones
LiAb-SFCANCER™ Human scFv & Fab PBMCs & BMMCs from 86 Human Donors
18 different cancers
Lung, Breast, Prostate, Colorectal, Pancreatic, Bladder, Stomach, Liver, Renal, Uterine, Ovarian, Skin, Thyroid, Lymphoma, Acute myeloid leukemia, Multiple myeloma, B-acute lymphoblastic leukemia (B-ALL), B-lymphoblastic lymphoma (B-LL)
6.81×10¹⁰ scFv & 6.72×10¹⁰ Fab
LiAb-SFAUTOIMM™ Human scFv & Fab PBMCs & BMMCs from Human Donors
12 different autoimmune diseases
Sjogren’s Syndrome, Psoriasis, Psoriatic Arthritis, Rheumatoid Arthritis, Systemic Lupus Erythematosus, Crohn’s Disease, Ulcerative Colitis, Ankylosing spondylitis, Autoimmune hepatitis, Scleroderma, Mixed connective tissue disease, Polymyositis
1.08×10¹¹ scFv & 1.06×10¹¹ Fab
Your custom library Your choice Your choice Your choice Your choice

Naïve Libraries for Maximum Versatility

Naïve libraries are good for low-immunogenic targets while being animal-free. The resulting antibodies are ideal for broad applications but will probably need affinity maturation.

Library Species Format Donors Diversity
LiAb-SFMAX™ Human scFv & Fab 368 healthy donors from 5 ethnic groups 5.37 x 10¹⁰ clones
LiAb-SFa™ Human scFv / 1.5 x 10⁹ clones
LiAb-Fab™ Human scFv / 2.00 x 10¹⁰ clones
Liab-VHHMAX™ Camel, llama, alpaca VHH 57 healthy animals 1.51 x 10¹⁰ clones
LiAb-SFDog™ Dog scFv & Fab 46 healthy animals from 6 breeds: Beagle, German Shepherd, Labrador, English Coonhound, Great Dane, Chinese Rural Dog 1.05 x 10¹⁰ scFv
1.01 x 10¹⁰ Fab
LiAb-SFCat™ Cat scFv & Fab 52 healthy animals from 8 breeds: Ragdoll, Maine Coon, Persian, Domestic Shorthair, Domestic Longhair, American Shorthair, Siamese, Bengal 1.32 x 10¹⁰ scFv
1.21 x 10¹⁰ Fab
LiAb-SFRab™ Rabbit scFv & Fab 40 healthy animals from 4 breeds: New Zealand White, Himalayan, Japanese White & Hare 1.09 x 10¹⁰ clones
LiPep-12 / Peptide 12-mer / 1.00 x 10⁹ clones
LiPep-7 / Peptide 7-mer / 1.00 x 10⁹ clones

Which library is right for your target? Selection depends on antigen format, conservation, immunogenicity, desired species and binder format, required affinity, and downstream assay. We can screen one library or combine complementary repertoires to maximise the probability of success.

Discuss your project

From antigen to validated binder

Our phage display and biopanning workflow

Each campaign is fully customized, but every project follows our rigorous, 5-step phase gate process to ensure maximum success.

1

Antigen QC and library selection

2.

4–6 rounds of biopanning with backup storage at each round

3.

ELISA screening of at least 96 single phage binders

4.

Sequencing and unique clone identification

5.

Delivery of sequences, detailed reports and IP

What you’ll receive

  • Comprehensive project report

    Complete description of methods,
    results and conclusions.

  • Lead antibody sequence

    The amino acid sequence of your
    selected binder.

  • Full IP ownership

    All agreed sequences transferred
    with no royalties or licensing fees.

Application-specific selection

Custom biopanning strategies for every antigen type

Every project starts with your target. We adapt the biopanning strategy and the library to the biological reality of your project. Below are the five approaches we deploy depending on your antigen and discovery objective.

    • Most soluble antigens

    Standard protein panning

    For soluble, correctly folded antigens. Campaigns generally use 4–6 panning rounds against immobilized target, followed by screening of at least 96 individual clones and sequencing of positive binders.

    • Peptides & small molecules

    Peptide panning

    The target can be conjugated to alternative carriers across rounds, combined with depletion against carrier alone. This reduces carrier-specific enrichment and favors recognition of the intended peptide or hapten.

    • Blocking & inhibition

    Neutralizing-binder strategy

    Ligand competition, masked-epitope depletion or competitive elution can enrich binders directed toward functional interfaces and active sites rather than non-functional epitopes.

    • Multi-species coverage

    Cross-reactive strategy

    Alternating cross-panning between related antigens enriches binders that recognize shared epitopes. Mixed-antigen rounds can be used first when the targets are highly divergent.

    • High selectivity

    Counter-screen strategy

    Pre-depletion against a structurally related counter-antigen before each round removes cross-reactive binders and drives selectivity toward the target epitope. Competitive elution in final rounds sharpens specificity further.

    • Need expert advice?

    Let’s choose the right strategy

    Every target is different. We’ll recommend the optimal library and biopanning strategy based on your antigen, application and project objectives.

    Request a project review

Counter-screen phage display results showing four selective anti-pHLA antibody clones identified from three libraries.

Case study: Counter-screen strategy

Selective anti-pHLA antibodies for CAR-T cell therapy in melanoma

An American pharmaceutical company was developing a next-generation CAR-T therapy targeting a melanoma-specific peptide-HLA complex.

The main challenge was selectivity. The antibody had to recognize the target peptide presented by the HLA molecule on tumour cells, while avoiding the same HLA molecule when presenting irrelevant or self-peptides.

To address this challenge, we applied a counter-screen phage display strategy using three complementary libraries:

  • LiAb-SFMAX™
  • LiAb-SFCANCER™
  • LiAb-SFAUTOIMM™

Results:

  • 3 proprietary libraries screened
  • 4 selective clones identified
  • Results delivered in 3 weeks

Read the case report Contact our Experts

Testimonials

Trusted by 9,000+ Researchers Worldwide

  • logo National cancer centre

    National Cancer Centre, Singapore

    “We have been working together with ProteoGenix since 2020. Using phage display, they helped our team to develop several antibodies with effective blocking effects. We are pleased with their services and look forward to continue working together with them as we advance our research and bring the biologics to clinical stage.”

    Prof Johnny Ong Chin-Ann, MD, PhD, Group leader

  • logo atyr pharma

    aTyr Pharma, USA

    “All three of the antibodies you delivered were reformatted into IgGs and worked well. Interestingly two were d1 binders, and one was a d1/d2 binder when we domain mapped them here. They were good “protein X” blocking antibodies. But none were “protein Y” blockers. They express reasonably well. Overall we are quite happy with them.”

    Senior scientist

  • logo nanyang technological university

    Nanyang Technological University, Singapore

    “ProteoGenix has been generous and sincere in supporting an academic laboratory like ours. They were able to identify several antibody sequences via phage display against a protein antigen and they screened twice more phages than initially planned to help us succeed in our project. ProteoGenix team was reactive and diligent in their replies and services.”

    Alvin Chew, Research Fellow

Scientific track record

Publications, clinical trial & patents

Publications

Nature – 2024
2 neutralizing antibodies (C9 & B3) with nM affinity against cancer target; C9 now in Phase I clinical trial LiAb-SFMAX™ (human naïve)

Read article

Publications

Clinical Cancer Research – 2024
Neutralizing antibody (A5) cross-reactive with 3 antigen conformations, nM affinity LiAb-SFMAX™ (human naïve)

Read article

Publications

Nature – 2025
Epitope mapping of SARS-CoV-2 Spike protein; mAbs developed using ProteoGenix phage display service with LiAb-SFCOVID-19™ LiAb-SFCOVID-19™

Read article

Publications
Clinical trial

NCT06645808 – 2024
Antibody C9 tested in cancer patients — Phase I LiAb-SFMAX™ (human naïve)

View trial

Phage display service FAQ

Need a quote or more information? Contact us!

    Cart (0 Items)

    Your cart is currently empty.

    View Products