End-to-End Antibody Discovery, Built Around Your Target
No single discovery platform suits every target. Conserved antigens, GPCRs, and multi-pass membrane proteins each break a different approach — so we start by choosing the route that fits the biology, not the one that fits our schedule. Immunization strategy, host species, and screening funnel are all designed around your antigen before a single animal is dosed.
Four integrated platforms — hybridoma, phage display, single B cell cloning, and affinity maturation — configured to the biology of your program. One team, from immunization to lead candidate.
One Partner. Multiple Discovery Paths.
Antibody discovery rarely follows a single trajectory. Target class, format, timeline, and developability requirements shape which platform fits your program.
ChemPartner integrates four complementary technologies, backed by in-house protein science, stable cell line development, functional assays, and structural biology. We configure the right approach for your target and transition between platforms when the science calls for it.
Antibodies Produced Annually
Scientific Team Members
Drugs to FDA/NDA Approval
Global Clients Served
Capability Modules
Deep Immunization Expertise for Diverse Target Classes
ChemPartner’s hybridoma platform combines comprehensive immunization strategies with a multi-tiered, high-throughput screening funnel.
We support mouse, rat, rabbit, hamster, alpaca/llama/camel, and fully human transgenic mice (Alloy; AceMouse) across a full range of immunogen formats — including recombinant proteins, cells, DNA, peptides, nanodisc, mRNA-LNP, VLP, and AAV particles — to maximize the probability of discovering high-affinity antibodies against any target class, including conserved and conformationally complex antigens.
- Multi-species immunization: mouse, rat, rabbit, hamster, alpaca/camel, fully human Tg mice (Alloy; AceMouse)
- Full immunogen flexibility: recombinant proteins, cells, peptides, DNA, mRNA-LNP, VLP, nanodisc, AAV
- Tolerance-breaking strategies (Anti-CD25, Anti-CD40, CpG, Mn²⁺) for conserved targets
- 384-plate high-throughput primary screening (Mirrorball/Acumen) against protein and cell-based antigens
- Multi-stage funnel: confirmatory FACS → cyno/mouse cross-reactivity → isoform selectivity → receptor-ligand blocking → functional assay
- Functional assay-driven subcloning, leads selected on biology, not binding titer alone
- BD Canto II, ForteBio Octet RED384, BD LSRFortessa, Carterra LSA, Freedom EVO, EL406
Proprietary, Royalty-Free Libraries for Any Format
ChemPartner’s phage display platform is built around proprietary, royalty-free antibody and peptide libraries — giving clients complete freedom to operate on resulting candidates without licensing encumbrance.
Libraries span naive, synthetic, and immune formats covering human scFv, VHH (nanobody), and peptide modalities, with combined diversity exceeding 10¹⁰ PFU per library.
- Solution-phase panning against biotinylated target proteins and/or overexpressing cell lines
- pH-dependent and epitope-biased panning strategies
- Primary screening: ELISA; secondary: off-rate ranking (ForteBio Octet)
- Total project timeline: 12–16 weeks to confirmed, characterized hits
- Affinity optimization libraries: alanine/histidine scanning, CDR-targeted mutagenesis
- Solution-phase panning against biotinylated target proteins and/or overexpressing cell lines
- pH-dependent and epitope-biased panning strategies
- Primary screening: ELISA; secondary: off-rate ranking (ForteBio Octet)
- Total project timeline: 12–16 weeks to confirmed, characterized hits
- Affinity optimization libraries: alanine/histidine scanning, CDR-targeted mutagenesis
- All ChemPartner phage display libraries are proprietary and royalty-free. Clients own all resulting IP without licensing cost or restriction — a critical differentiator vs. commercial library providers.
Functional Antibodies in Days, Not Weeks
ChemPartner’s Boston Center of Excellence operates the Beacon™ platform — one of the most powerful tools in antibody discovery for identifying rare, functionally active antibodies directly from single B cells.
The system uses light-based optofluidic technology to manipulate thousands of individual B cells in parallel, running binding and functional assays in-pen before committing to cloning.
- In-pen binding and blocking assays: 4 hours to overnight from cell load to exported hits
- Functional hit identification (blocking, signaling, agonism/antagonism) in 1 day
- Multiplex or sequential assay capability within a single run
- Thousands of individual cells screened in parallel — rare clones that would be diluted out in hybridoma are captured
- Direct sequence recovery from functional B cell clones
- In a head-to-head PD-L1 comparison, single B cell cloning via Beacon delivered significantly more functional antibodies than hybridoma — from the same immunization, in less time to sequence.
- Published: Rapid discovery of a diverse panel of novel cross-reactive antibodies against uPAR in triple-negative breast cancer — antibodies that hybridoma missed. Khan et al., MABS 2023, 15(1):2184197. DOI: 10.1080/19420862.2023.2184197
Structure-Guided Engineering to Push Your Lead to Therapeutic Grade
Once leads are identified, ChemPartner’s engineering team applies rational design and library-based strategies to drive affinity, selectivity, and developability to IND-enabling specifications. Structure-based computational approaches work in concert with phage display affinity libraries and biophysical characterization to achieve multi-order-of-magnitude improvements.
- Alanine and histidine scanning mutagenesis to map permissive CDR sites
- Structure-based, computation-aided affinity maturation
- CDR-targeted affinity library generation and phage display-driven optimization
- Up to 295-fold improvement in peptide affinity maturation (SPR-validated)
- 70-fold affinity improvement demonstrated for IL-1β mAb — combining mutations from two CDRs (ChemPartner Patent CN104341501B)
- 42.8-fold improvement in mono-cyclic peptide affinity maturation
- Developability screening is embedded throughout the maturation process — not applied as a late-stage filter. Assessment covers: in silico hotspot analysis and immunogenicity prediction; biophysical profiling (SEC, DSF, HIC-HPLC, AC-SINS, Uncle); polyspecificity (BVP/dsDNA/insulin ELISA); freeze-thaw, pH, thermal, and high-concentration stability.
One Platform. Seamlessly Integrated.
Antibody discovery doesn’t end at hit identification. ChemPartner’s program architecture means your antibody moves from discovery through lead optimization, developability screening, and into protein production — without switching partners, restarting assays, or losing institutional knowledge about your target.
From a single point of contact, you get full scientific depth at every stage — and continuity from the scientist who ran your first ELISA to the one who authors your IND module.
Explore the Full Range of Development and Manufacturing Capabilities
Multi-species immunization and high-throughput, functionally-driven screening.
Royalty-free proprietary libraries. scFv, VHH, and peptide formats. IP freedom guaranteed.
Beacon® OptoSelect™ — functional antibody identification in a single day.
Tg mouse platforms (Alloy; AceMouse) for fully human therapeutic antibody programs.
Structure-guided engineering. Up to 295-fold affinity improvement. IP-backed methodology.
Integrated discovery programs and specialty antibody services tailored to your timeline.
Ready to Discuss Your Antibody Program?
Tell us your target and timeline. Our scientists will configure the right discovery approach and get back to you within one business day.