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Built from a dual source, our library captures up to 90% of the human antibody-producing B cells. This ensures access to clinically relevant targets, including self-antigens, neoantigens, and MHC–peptide complexes, and many targets that synthetic libraries fail to reach.
The LiAb-SFCANCER™ is built from 86 cancer patients across 18 indications, providing an exceptionally diverse repertoire: 6.81×10¹⁰ scFv and 6.72×10¹⁰ Fab clones.
Our phage display library includes rare malignancies—B-lymphoblastic leukemia (B-ALL), B-lymphoblastic lymphoma (B-LL), and multiple myeloma— characterized by a high proliferation of pre-B cells that recognize self-antigens, making LiAb-SFCANCER™ a unique library worldwide.
We deliver a minimum of three validated binders, giving you backup candidates to secure your success.
Save valuable time with a streamlined sequence-to-antibody workflow without compromising quality or performance.
Without royalties or licensing fees, you maintain full control over your downstream development.
See how this unique phage display library accelerates progress across multiple oncology use cases. By providing human cancer-specific antibodies with low engineering requirements and reduced immunogenicity risks, you accelerate the development of your antibody against challenging targets and its transition to the preclinical stage.
Explore how we designed an antibody against a target barely visible to the immune system.
Explore how innovative phage display technologies, powered by our antibody library derived from cancer patients, can accelerate the development of novel therapeutics while saving time and reducing animal use.
Discover the relevance of our LiAb-SFCANCERTM Library for developing antibodies against cancer antigens.