Quantifying biomolecular interactions with high precision for drug discovery and target validation
Our molecular binding assays provide quantitative measurements of interactions between small molecules, peptides, and proteins—critical for identifying promising drug candidates and understanding their mechanism of action. These assays enable precise determination of binding affinity (Kd), specificity, and kinetic parameters (kon/koff) to support rational drug design and target validation.
Homogeneous and heterogeneous fluorescence assays including FRET, TR-FRET, and fluorescence polarization techniques for rapid screening of compound libraries.
Label-free technology for real-time monitoring of biomolecular interactions, providing kinetic and affinity data without requiring fluorescent tags.
Direct measurement of binding thermodynamics (ΔH, ΔS, ΔG) to characterize the energy landscape of molecular interactions.
We offer collaborative assay development services tailored to specific therapeutic targets and research questions.
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