6-(6-(5-((3aS,4S,6aR)-2-Oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)hexanamido)hexanoic acid

N-Biotinylcaproylaminocaproic acid serves as a crucial molecular linker in bioconjugation and protein labeling experiments. Its primary function involves attaching the biotin group covalently to specific amino acid residues on target proteins. This attachment enables subsequent purification, detection, or immobilization of the labeled proteins. In biological research, N-Biotinylcaproylaminocaproic acid facilitates the exploration of protein-protein interactions, protein localization, and protein function. By allowing precise and selective protein labeling, it supports advancements in molecular biology, biochemistry, and cell biology. This compound plays a pivotal role in modifying proteins for a wide range of analytical and investigative purposes in experimental settings.