CheMatech provides tailored bioconjugation services for the design and preparation of targeted conjugates for nuclear medicine applications. Leveraging our broad portfolio of chelators and functionalized building blocks, we support the development of bioconjugates optimized for stability, targeting efficiency, and in vivo performance.
Selecting the appropriate chelator is critical to ensure high complex stability, preserve the biological activity of the targeting vector, and minimize radionuclide release in vivo. Our team supports you in identifying the most suitable chelation and conjugation strategy based on your radionuclide, vector, and intended application.
We offer bioconjugation solutions for a wide range of biomolecules (mAbs, Fab, nanobodies, VHHs, etc.), using chemistries adapted to:
- Cysteine residues
- Lysine residues
- Click chemistry approaches
Both the chelator and the conjugation strategy can be tailored to your specific requirements, enabling the development of optimized conjugates aligned with your project objectives.