Propargyl-O-C1-amido-PEG2-C2-NHS ester is a non-cleavable linker designed for antibody-drug conjugates (ADCs) that facilitates precise molecular attachment. This 2-unit PEG linker incorporates an alkyne group, enabling the copper-catalyzed azide-alkyne cycloaddition (CuAAC) with azide-containing compounds. Its unique structure supports enhanced stability and bioactivity in various biochemical applications, making it a valuable reagent for research in targeted therapeutics and drug delivery systems.
Propargyl-O-C1-amido-PEG2-C2-NHS ester is a non-cleavable linker designed for antibody-drug conjugates (ADCs) that facilitates precise molecular attachment. This 2-unit PEG linker incorporates an alkyne group, enabling the copper-catalyzed azide-alkyne cycloaddition (CuAAC) with azide-containing compounds. Its unique structure supports enhanced stability and bioactivity in various biochemical applications, making it a valuable reagent for research in targeted therapeutics and drug delivery systems.
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