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Product Introduction
TAMRA Hydrazide is a reactive form of bright yellow dye that used to generate a stable fluorescence signal in bioimaging. The maxima of Ex/Em values are at 544/576 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. Hydrazides can label aldehyde and ketone through reductive amination reaction to form an imine linkage. The main labeling target for hydrazides are free reducing sugars on biomolecules, and prior to conjugation, primary and secondary alcohols on polysaccharide and glycoprotein are usually oxidized to aldehyde and ketone. We offer TAMRA hydrazide for labeling of polysaccharide, glycoprotein and other biomolecules bearing aldehyde or ketone.
Chemical Information
Product Specification
Application
Chemical Information
| Solubility | DMF, DMSO |
| Appearance | Red solid |
Product Specification
| Excitation | 544 |
| Emission | 576 |
| Storage | -20 °C, protect from light |
Application
TAMRA Hydrazide is a reactive TAMRA-based fluorescent labeling reagent designed for forming stable hydrazone conjugates with aldehyde-functional biomolecules and materials. Its bright red/orange fluorescence makes it widely used for tracking biomolecule labeling, monitoring conjugation outcomes, and preparing fluorescence imaging reagents. The hydrazide handle enables convenient post-functionalization of aldehydes introduced by oxidation or periodate-type workflows, supporting downstream microscopy, gel-based readouts, and fluorescence assays.
1. Aldehyde Biomolecule Labeling
TAMRA Hydrazide is commonly used to fluorescently tag aldehyde-bearing proteins, peptides, and glycoconjugates for visualization and analytical confirmation of labeling. Researchers typically apply it after generating aldehydes on biomolecules (for example via controlled oxidation of carbohydrate moieties or other aldehyde-introduction strategies), then use the resulting TAMRA-hydrazone conjugates for fluorescence imaging and fluorescence-based quantification. This workflow is frequently adopted in chemical biology and biomaterials studies where labeling efficiency and conjugate integrity need to be monitored alongside the biological experiment.
2. Fluorescent Conjugate Tracing
TAMRA Hydrazide supports preparation of fluorescent conjugates for tracking biomolecule uptake, distribution, and association in cell and material studies. In practice, investigators use TAMRA-labeled glycans, oxidized biomolecule carriers, or aldehyde-functional polymers to follow conjugate localization by fluorescence microscopy and to assess labeling consistency across experimental batches. Because the reagent is designed for aldehyde-reactive coupling, it is also used to compare labeling conditions, verify conjugate formation, and generate fluorescent standards for assay development where a TAMRA emission channel is already established.
3. Gel And Blot Fluorescence Readout
TAMRA Hydrazide is frequently incorporated into workflows that require sensitive fluorescence readout of labeled biomolecules on electrophoretic gels and membrane blots. After conjugation to aldehyde-containing targets, TAMRA fluorescence enables visualization of labeled bands and assessment of relative labeling levels without relying on enzymatic or colorimetric detection. This makes the reagent useful for method development in bioconjugation, glycan labeling optimization, and quality control of fluorescent conjugates prior to downstream imaging or binding studies.
4. Biomaterial And Surface Functionalization
TAMRA Hydrazide is used to create fluorescently labeled biomaterial surfaces and polymer coatings through hydrazone formation with aldehyde-functional materials. Researchers apply TAMRA labeling to hydrogels, oxidized polymer backbones, and aldehyde-terminated surfaces to enable imaging of material distribution, verify functionalization uniformity, and support fluorescence-based characterization of engineered matrices. In biomaterials development, the reagent helps connect chemical modification steps to measurable fluorescent outputs that can be evaluated by microscopy and other fluorescence instrumentation.
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