BCN-PEG3-OH is a non-cleavable linker specifically designed for antibody-drug conjugate (ADC) synthesis. As a click chemistry reagent, it features a bicyclo[6.1.0]nonyne (BCN) moiety that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. This compound supports robust conjugation strategies, enhancing the delivery of cytotoxic agents in targeted cancer therapies. Its efficiency makes it an invaluable tool in the development of ADCs for various research applications.
BCN-PEG3-OH is a non-cleavable linker specifically designed for antibody-drug conjugate (ADC) synthesis. As a click chemistry reagent, it features a bicyclo[6.1.0]nonyne (BCN) moiety that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. This compound supports robust conjugation strategies, enhancing the delivery of cytotoxic agents in targeted cancer therapies. Its efficiency makes it an invaluable tool in the development of ADCs for various research applications.
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