
TAMRA NHS ester, 5-isomer | CAS 321862-17-3
| Catalog Number | R01-0037 |
| Category | NHS Esters |
| Molecular Formula | C29H25N3O7 |
| Molecular Weight | 527.53 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
TAMRA (tetramethylrhodamine) is a xanthene dye of rhodamine series. This fluorophore is being used for quite a long time for the preparation of dual labeled qPCR TaqMan oligonucleotide probes containing TAMRA and fluorescein (FAM).Just like many other xanthene fluorophores, TAMRA is a available as two isomers (5-and 6-isomer) which have nearly identical optical properties. This product is an isomerically pure 5-TAMRA.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | NMR 1H, HPLC-MS (95%) |
| Solubility | good in DMF, DMSO, low in water |
| Appearance | dark colored solid |
Product Specification
| ε, L⋅mol-1⋅cm-1 | 84000 |
| Fluorescence Quantum Yield | 0.1 |
| Excitation | 541 |
| Emission | 567 |
| Storage | 12 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. Desiccate. |
Application
TAMRA NHS ester, 5-isomer is a fluorescent NHS-ester (N-hydroxysuccinimide ester) designed for amine-reactive bioconjugation via widely used click-compatible labeling workflows. As a rhodamine-based dye, it provides strong visible fluorescence for tracking biomolecules, surfaces, and materials after covalent attachment to primary amines such as lysine residues and N-termini. The 5-isomer form is commonly selected in labeling pipelines where consistent dye performance and spectral behavior are important for imaging, assay development, and reagent characterization.
1. Antibody And Protein Labeling
TAMRA NHS ester, 5-isomer is routinely employed to generate fluorescently labeled antibodies, enzymes, and protein probes by covalently coupling to accessible lysine side chains and N-terminal amines. Researchers use this reagent to prepare binding reagents for flow cytometry, fluorescence microscopy, and protein localization studies, where stable dye attachment helps maintain signal during washing and incubation steps. Because the NHS-ester reacts under standard aqueous labeling conditions, it fits seamlessly into routine protein conjugation workflows used in chemical biology and molecular imaging labs.
2. Peptide And Biomolecule Tagging
TAMRA NHS ester, 5-isomer is well suited for labeling peptides, oligonucleotide-associated peptides, and other amine-containing biomolecules to create fluorescent substrates and tracking tools. In chemical biology, it is commonly used to introduce a bright, spectrally distinct fluorophore for monitoring binding, uptake, or trafficking in experimental assay formats that rely on covalent dye attachment rather than passive adsorption. The dye’s NHS-ester functionality also supports straightforward incorporation into multi-component labeling strategies where the fluorescent tag must remain stable across buffer exchanges and downstream handling.
3. Surface And Material Functionalization
TAMRA NHS ester, 5-isomer is frequently used to fluorescently functionalize biomaterials and solid supports that present reactive amines, including amine-terminated surfaces, polymer coatings, and porous matrices used in imaging and materials characterization. By enabling covalent attachment of the dye to surface-bound amine groups, the reagent helps researchers visualize coating uniformity, quantify surface labeling, and generate fluorescent readouts for material assembly and stability studies. This application is particularly common in biomaterials science where fluorescent surface markers are used to validate fabrication steps and to support microscopy-based characterization.
4. Diagnostic Reagent Development
TAMRA NHS ester, 5-isomer is commonly incorporated into research diagnostic reagent platforms that require fluorescent labeling of capture molecules, affinity reagents, or assay components. Labeling with an NHS-ester facilitates covalent conjugation to amine-bearing biomolecules used in immunoassays, binding assays, and multiplex fluorescence workflows, supporting robust signal generation and reproducible reagent behavior across assay runs. In diagnostic reagent development, the dye is also used to create reference standards and labeled controls for assay optimization and reagent verification in fluorescence-based detection formats.
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