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Product Introduction
FAM Hydrazide is a reactive form of bright green dye used to generate a stable fluorescence signal in bioimaging. The maxima of Ex/Em values are at 492/519 nm, similar to that of Alexa 488 and Cy2. FAM might be excited using 488 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 FAM hydrazide for labeling of polysaccharide, glycoprotein and other biomolecules bearing aldehyde or ketone.
Chemical Information
Product Specification
Application
Chemical Information
| Solubility | DMF, DMSO |
| Appearance | Yellow solid |
Product Specification
| Excitation | 492 |
| Emission | 492 |
| Storage | -20 °C,protect from light |
Application
FAM Hydrazide is a fluorescein (FAM) hydrazide dye designed for fluorescent labeling through hydrazone formation with carbonyl-containing targets. In conjugation workflows, the hydrazide functionality enables attachment to aldehydes and ketones generated on biomolecules or engineered onto surfaces, providing a bright, visible fluorescence tag for imaging and assay development. Its fluorescein core supports common excitation/emission detection schemes used in fluorescence microscopy and plate-based readouts.
1. Aldehyde Biomolecule Labeling
FAM Hydrazide is widely used to fluorescently tag aldehyde-bearing biomolecules, including oxidized carbohydrates, glycoproteins, and lipid-derived carbonyls, where hydrazone formation provides a practical route to incorporate a fluorescein reporter. Researchers employ this labeling strategy for fluorescence imaging of labeled biomolecular conjugates, for tracking biomolecule binding events in solution, and for preparing fluorescent standards used in assay development. In chemical biology and glycobiology workflows, the reagent is often selected when carbonyl functionality is introduced enzymatically or chemically and a robust fluorescent readout is needed for downstream analysis.
2. Fluorescent Probe Construction
FAM Hydrazide serves as a key fluorescent building block for constructing carbonyl-responsive probes and labeling reagents used in molecular imaging and fluorescence-based detection development. In probe design workflows, hydrazide chemistry is leveraged to install a fluorescein reporter onto probe scaffolds that present aldehyde/ketone handles, enabling visualization of probe distribution and incorporation into target-containing materials. Teams developing fluorescence assays for biomolecule tracking, reaction monitoring, or labeling verification frequently use FAM Hydrazide to generate fluorescent conjugates that can be quantified by standard fluorescence instrumentation.
3. Surface and Material Functionalization
FAM Hydrazide is used to functionalize carbonyl-containing biomaterial surfaces and polymer materials with a fluorescein tag for microscopy and material characterization. When materials are prepared with aldehyde or ketone groups, hydrazide coupling can introduce a fluorescent label that helps visualize surface coverage, coating uniformity, and localization of biomolecule layers during material assembly. This application is common in biomaterials science and surface engineering, where fluorescent labeling supports rapid qualitative assessment of functionalization steps and enables comparative studies across different surface chemistries using fluorescence imaging or plate-based fluorescence measurements.
4. Flow Cytometry Labeling Verification
FAM Hydrazide is frequently applied as a fluorescent labeling reagent to verify carbonyl-mediated labeling steps during cell and particle staining workflows, particularly when labeling intermediates or conjugation efficiency need to be assessed by flow cytometry. Researchers use the fluorescein signal to monitor the presence of aldehyde/ketone-derived labeling on carrier particles, conjugated reagents, or cell-associated constructs prepared with carbonyl handles. This use supports assay development and reagent optimization by providing a straightforward fluorescence readout compatible with common flow cytometry detection channels used for fluorescein-family dyes.
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