Incorporate multiple target selections, counter-target screening and fine tune selection to specific sites on your target
Build super-large peptide libraries tailored for specific targets or therapeutic modality, offering a wide array of chemistries, structures, and affinities.
Accelerate the discovery process with FACS-based screening, identifying and refining low affinity binders for fast optimization.
Opitimise and expand your hit with access to Orbit's peptide chemistry expertise. Test linkers and ligase combinations to turn your hit peptide into a lead.