
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
TAMRA Azide is a copper (I)-catalyzed azide-alkyne cycloaddition (CuAAC) reagent of bright yellow dye that used to generate a stable fluorescence signal in bioimaging. The maxima of Ex/Em values are at 547/573 nm, similar to that of DyLight 549, ATTO 550 and Cy 3. TAMRA might be excited using 543 or 546 nm laser line and displays good optical property. The azide reactive group is connected to the dye through an amino propyl linkage. TAMRA azide couples with an alkyne to form 1,4-disubstituted 1,2,3-triazole inside of living systems without interfering native biochemical processes. Prior to perform CuAAC, the alkyne functionality should be introduced onto counterpart biomolecule by means of chemical or genetic modification. We offer TAMRA Azide as a click chemistry reagent dye for cellular imaging and nucleotide functionalization.
Chemical Information
Product Specification
Application
Chemical Information
| Solubility | DMF |
| Appearance | Red solid |
Product Specification
| Excitation | 547 |
| Emission | 573 |
| Storage | -20 °C, protect from light |
Application
TAMRA Azide is a TAMRA-based fluorescent labeling building block bearing an azide functional group, enabling bioorthogonal conjugation workflows that install a bright red-orange fluorophore onto biomolecules and materials. In fluorescence applications, the azide handle is used to couple TAMRA into complex targets while preserving the dye's utility for microscopy and fluorescence readouts, including probe and conjugate construction for assay development.
1. Click-Based Biomolecule Labeling
TAMRA Azide is used by chemical biology and glycobiology groups to fluorescently tag proteins, peptides, and other azide-compatible biomolecules via click chemistry workflows, supporting downstream fluorescence imaging and quantitative assays. Researchers commonly incorporate the TAMRA fluorophore into labeling schemes to visualize binding events, track conjugate uptake in model systems, or generate fluorescent standards for assay calibration. The azide functionality makes it a convenient fluorophore payload for constructing labeled reagents without introducing the dye directly during protein expression, which is particularly useful in workflows where post-labeling control is required.
2. Fluorescent Probe Construction
TAMRA Azide is frequently employed in fluorescent probe development where a TAMRA reporting group is needed as part of a larger sensing or detection reagent. Probe designers use the azide handle to install TAMRA onto targeting ligands, scaffold molecules, or assay components, enabling modular construction of fluorescence readouts for microscopy-based studies and plate-reader measurements. In practice, this supports the creation of labeled affinity reagents, imaging probes, and multi-component detection systems where the fluorophore must be appended at a defined stage of reagent assembly.
3. Surface And Polymer Functionalization
TAMRA Azide is used in materials research to introduce a fluorescent tag onto polymer backbones, hydrogels, and surface-modified substrates through click-compatible coupling strategies. Biomaterials groups leverage the dye installation to visualize coating uniformity, map surface coverage, and monitor biomaterial interactions under fluorescence microscopy. Because the TAMRA moiety provides a robust red-orange fluorescence signal, TAMRA Azide is also used to generate fluorescently labeled materials for method development in imaging workflows and for comparative studies of surface chemistry.
4. Fluorescence Microscopy Labeling
TAMRA Azide supports fluorescence microscopy workflows where researchers require a red-orange fluorophore for cellular and molecular visualization. Imaging teams use TAMRA-labeled conjugates prepared from TAMRA Azide to track labeled biomolecules, follow localization patterns in fixed samples, and validate conjugation outcomes prior to more complex experimental steps. The azide handle enables consistent fluorophore incorporation into labeling reagents, which is valuable when building microscopy-compatible probes and conjugates for co-localization studies with other fluorescent markers.
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry