
AF568 azide, 6-isomer
| Catalog Number | R01-0045 |
| Category | Alexa Fluor |
| Molecular Formula | C36H34N6K2O10S2 |
| Molecular Weight | 853.02 |
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Product Introduction
AF568 is a fluorescent dye. Its excitation peak is at 572 nm and its emission peak at 598 nm. AF568 azide is a photochemically stable, specific, and highly efficient tool for labeling biomolecules. It is water soluble and insensitive to pH changes between pH 4 and pH 10. The reaction conditions do not require high temperature or pressure.,Labeling with AF568 azide via Click Chemistry is a powerful technique for the production of bioconjugates. Thus, AF568 azide is an excellent tool for imaging purposes, including fluorescent microscopy and flow cytometry, where label brightness and photostability are essential.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | NMR 1H, HPLC-MS (95%) |
| Solubility | Good in water, DMF, DMSO |
| Appearance | Dark colored solid |
Product Specification
| CF260 | 0.4 |
| CF280 | 0.32 |
| Fluorescence Quantum Yield | 0.912 |
| Mass Spec M+ Increment | 776.2 |
| Excitation | 572 |
| Emission | 598 |
| Storage | Storage: 24 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
AF568 azide, 6-isomer is a fluorescent azide derivative of the AF568 dye family designed for copper-free click chemistry labeling workflows. With an azide handle for bioorthogonal conjugation and an AF568 emission profile commonly used in red fluorescence imaging, this reagent supports the construction of fluorescent conjugates for microscopy, flow cytometry, and fluorescence-based assay development where robust dye attachment is required. Researchers use the 6-isomer form to access consistent labeling performance in azide-based probe and reagent pipelines.
1. Biomolecule Azide Labeling
AF568 azide, 6-isomer is used by chemical biology and protein engineering groups to install red fluorescence tags onto biomolecules through azide-alkyne click conjugation strategies. In labeling workflows, the azide functionality enables attachment to alkyne-bearing targeting ligands, affinity reagents, peptides, and proteins, producing fluorescent conjugates for downstream imaging or binding studies. This format is particularly convenient when the dye must be introduced as a defined clickable handle rather than as a pre-conjugated dye, supporting modular probe construction for assay development and molecular imaging reagent optimization.
2. Fluorescence Microscopy Staining
AF568 azide, 6-isomer is applied in fluorescence microscopy to generate red-emitting staining reagents for cellular imaging experiments where click-assembled labeling is preferred. Typical use cases include preparing fluorescent conjugates for labeling cell-associated targets, tracking biomolecular interactions on surfaces, and visualizing labeled biomolecule distributions in fixed or prepared samples. The azide handle allows researchers to couple the dye to alkyne-functional biomaterials or targeting constructs, enabling flexible staining reagent design that aligns with multicolor imaging workflows using red detection channels.
3. Flow Cytometry Conjugates
AF568 azide, 6-isomer supports flow cytometry workflows by enabling the preparation of red-fluorescent conjugates using azide-based click labeling. Researchers use the dye to tag alkyne-functional antibodies, binders, or other fluorescence-reporting constructs to quantify labeled populations by fluorescence intensity readout. This approach is commonly used in panel development where modular conjugation helps standardize reagent batches and supports consistent incorporation of the AF568 fluorophore into flow cytometry-compatible labeling reagents.
4. Fluorescent Probe Construction
AF568 azide, 6-isomer is frequently incorporated into fluorescent probe development pipelines to create clickable reporter components for custom detection assays. In molecular imaging reagent and biosensor R&D, the azide functionality is leveraged to attach the AF568 fluorophore to recognition scaffolds, linkers, or surface-anchored platforms that contain complementary clickable groups. This enables rapid iteration of probe architectures for fluorescence readouts, including conjugate-based assays and imaging probes where the dye must be introduced as a defined clickable reporter rather than through non-specific dye labeling.
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