Description
N-(azido-PEG4)-biocytin is a biotin PEG linker featuring a carboxylic group and an azide group. The carboxylic group readily forms stable, irreversible amide bonds with primary amino (-NH2) groups. The azide group allows for conjugation with alkyne moieties in Cu(I)-catalyzed Click Chemistry reactions or DBCO moieties in copper-free Click Chemistry reactions, forming stable triazole linkages. Additionally, the inclusion of a hydrophilic PEG spacer enhances the solubility of the biotin-conjugated molecules in aqueous media.
Applications
N-(azido-PEG4)-biocytin is widely employed in bioconjugation and labeling applications, including protein labeling, cell surface modification, and chemical biology studies. Its versatility allows for precise and efficient biotinylation of biomolecules such as proteins, peptides, and nucleic acids, facilitating various downstream applications such as affinity purification, immunoprecipitation, and fluorescence microscopy.