Fluorophore Azides/Alkynes [Conjugation Chemistry/Click Chemistry]

Fluorophore Azides/Alkynes [Conjugation Chemistry/Click Chemistry] — includes fluorophore molecules functionalized with azide, alkyne, or dibenzocyclooctyne (DBCO) groups, including cyanine, coumarin, pyrene, and fluorescein derivatives. This group is designed to participate in azide-alkyne cycloaddition reactions as part of bioorthogonal conjugation chemistry.

Fluorophore Azides/Alkynes [Conjugation Chemistry/Click Chemistry] are used to label biomolecules such as proteins, peptides, or nucleic acids through click reactions, either without a catalyst or with a copper catalyst, producing fluorescent conjugates for imaging and detection. Bioorganic chemistry and chemical biology researchers utilize the variety of fluorophores and reactive groups in this category to tune detection wavelengths and compatibility with biological systems.

Example products in this collection: TCI U0167 1394116-40-5 Sulfo-Cyanine 5 DBCO, TCI E0939 34993-56-1 1-Ethynylpyrene, TCI U0166 1345823-20-2 Sulfo-Cyanine5-Alkyne, TCI F1243 412319-45-0 6-FAM-PEG3-Azide, TCI A3306 817638-68-9 3-Azido-7-hydroxycoumarin, TCI P2226 1115084-83-7 1-[(2-Propynyloxy)methyl]pyrene, TCI A2791 1006061-57-9 1-(Azidomethyl)pyrene.

Pay attention to the type of reactive group (azide, alkyne, or DBCO), the spectral characteristics of the fluorophore such as excitation-emission wavelengths, and solubility in aqueous media for bioorthogonal applications. All products are genuine Tokyo Chemical Industry (TCI) Japan products, with purity, packaging, and storage conditions listed on each item's page.

Other parallel categories under Conjugation Chemistry/Click Chemistry, often used together in a single laboratory workflow:

Back to Conjugation Chemistry/Click Chemistry. For large-volume procurement, special packaging, or specific grades, contact the AMI Scientific team — the official TCI Japan distributor in Indonesia — for availability checks and direct lead times from Japan.

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