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*For research and further manufacturing use only, not for direct human use.
Structure of 2112738-13-1
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Mal-amido-PEG2-Val-Cit-PAB-PNP features a cleavable Val-Cit dipeptide linker paired with a PAB-PNP payload, enabling site-specific conjugation via maleimide-thiol chemistry. This construct delivers high stability in circulation while ensuring efficient intracellular release, ideal for antibody-drug conjugate development.
Mal-amido-PEG2-Val-Cit-PAB-PNP serves as a robust linker for antibody-drug conjugates, enabling site-specific payload attachment via maleimide-thiol chemistry. The PEG2 spacer enhances solubility and stability, while the Val-Cit dipeptide provides protease-sensitive cleavage in target cells. This construct facilitates efficient drug release and demonstrates compatibility with standard bioconjugation workflows.
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Lot numbers can be found on the outside label of a product: