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Product Introduction
TAMRA ADIBO is a strain-promoted azide-alkyne cycloaddition (SPAAC) reagent of bright yellow dye that used to generate a stable fluorescence signal in bioimaging. The maxima of Ex/Em values are at 543/575 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 TAMRA ADIBO couples with an azide to form 1,4-disubstituted 1,2,3-triazole inside of living systems without using any coupling reagents or catalyst nor interfering native biochemical processes. Prior to perform SPAAC, the azide functionality should be introduced onto counterpart biomolecule by means of chemical or genetic modification. We offer TAMRA ADIBO 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 | 543 |
| Emission | 575 |
| Storage | -20 °C, protect from light |
Application
TAMRA ADIBO is a TAMRA-based fluorescent labeling reagent designed for conjugation workflows that benefit from an activated, dye-bearing scaffold. Its red-emitting fluorescence is commonly leveraged in fluorescence microscopy, gel-based and plate-based readouts, and nucleic-acid-adjacent labeling strategies where robust signal from the TAMRA chromophore is required. The ADIBO functionality supports installation onto primary amines under bioconjugation conditions, enabling preparation of fluorescent conjugates for downstream imaging and assay development.
1. Biomolecule Fluorescent Labeling
TAMRA ADIBO is used by chemical biology and proteomics groups to generate TAMRA-labeled biomolecules for fluorescence tracking and analytical readouts. Researchers typically install the dye onto proteins, peptides, and other amine-containing targets to create fluorescent conjugates for binding studies, workflow optimization, and visualization of labeled reagents in complex mixtures. In practice, the reagent is a convenient choice when a TAMRA reporter is needed for red-channel imaging and when amine-reactive conjugation is the preferred labeling handle for preparing fluorescent probes or standards.
2. Fluorescence Microscopy Staining
TAMRA ADIBO supports fluorescence microscopy workflows where red-emitting labeling is used to visualize labeled biomolecules associated with cells or biomaterials. Lab teams often prepare TAMRA-conjugated ligands, affinity reagents, or extracellular components and then use these conjugates to monitor localization patterns by widefield or confocal imaging. The dye's bright red fluorescence makes it practical for multicolor experiments that include other fluorophores, enabling researchers to track labeled components against cellular or scaffold backgrounds in fixed-sample imaging studies.
3. Flow Cytometry Fluorescent Conjugates
TAMRA ADIBO is applied in flow cytometry reagent development to produce TAMRA-labeled biomolecules for cell-associated readouts. Researchers use TAMRA-conjugates to quantify binding of fluorescent reagents to cell surfaces or to label intracellular targets after appropriate sample preparation, relying on the red emission of TAMRA for gating and population analysis. This use case is particularly common in assay development and method validation, where stable, amine-based fluorescent labeling provides a straightforward route to generate consistent reagents for instrument workflows.
4. Nucleic-Acid-Adjacent Labeling
TAMRA ADIBO is also used to prepare TAMRA-labeled components that participate in nucleic-acid-adjacent assay formats, including labeling of amine-bearing oligonucleotide conjugates or nucleic-acid-associated proteins used as reporters. Molecular biology and diagnostics research teams often incorporate TAMRA fluorescence into probe construction strategies where red emission is advantageous for multiplexing or for compatibility with existing instrument channels. In these workflows, the reagent's amine-reactive conjugation capability helps generate fluorescent conjugates used for monitoring binding events and for constructing fluorescence-based nucleic-acid analytical tools.
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