
AF 568 alkyne
| Catalog Number | R01-0458 |
| Category | Alexa Fluor |
| Molecular Formula | C36H31K2N3O10S2 |
| Molecular Weight | 807.97 |
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Product Introduction
AF 568 alkyne derivate is an effective tool for labeling purposes. It is easily detected in the ROX channel with a high signal-to-noise ratio in different biological samples. Bioconjugation with AF 568 alkyne presents a powerful technique for the production of fluorescently labeled biomolecules.
Chemical Information
Product Specification
Application
Chemical Information
| IUPAC Name | dipotassium;[13-[2-carboxy-4-(prop-2-ynylcarbamoyl)phenyl]-7,7,19,19-tetramethyl-17-(sulfonatomethyl)-2-oxa-6,20-diazapentacyclo[12.8.0.03,12.05,10.016,21]docosa-1(22),3(12),4,8,10,13,15,17,20-nonaen-9-yl]methanesulfonate |
| SMILES | CC1(C=C(C2=CC3=C(C=C2N1)OC4=CC5=NC(C=C(C5=CC4=C3C6=C(C=C(C=C6)C(=O)NCC#C)C(=O)O)CS(=O)(=O)[O-])(C)C)CS(=O)(=O)[O-])C.[K+].[K+] |
| InChI | InChI=1S/C36H33N3O10S2.2K/c1-6-9-37-33(40)19-7-8-22(25(10-19)34(41)42)32-26-11-23-20(17-50(43,44)45)15-35(2,3)38-28(23)13-30(26)49-31-14-29-24(12-27(31)32)21(18-51(46,47)48)16-36(4,5)39-29;;/h1,7-8,10-16,38H,9,17-18H2,2-5H3,(H,37,40)(H,41,42)(H,43,44,45)(H,46,47,48);;/q;2*+1/p-2 |
| InChIKey | MEKLAWYEJGIWMU-UHFFFAOYSA-L |
| Appearance | Violet Powder |
Product Specification
| Excitation | 572 |
| Emission | 598 |
Application
AF 568 alkyne is a fluorescent alkyne reagent designed for click chemistry-based conjugation, enabling efficient incorporation of an AF 568 fluorophore into biomolecules, polymers, and functional materials. With the alkyne handle, it is commonly used in copper-catalyzed azide-alkyne cycloaddition workflows to generate fluorescent labeling reagents for microscopy and fluorescence readouts. The AF 568 dye format supports a broad range of fluorescence imaging and labeling experiments where robust covalent attachment is required.
1. Biomolecule Fluorescent Labeling
AF 568 alkyne is frequently used by chemical biology and fluorescence microscopy groups to covalently label proteins, peptides, and other biomolecules that have been functionalized with azide groups. Researchers incorporate the dye into azide-bearing biomolecules to create defined fluorescent conjugates for tracking binding, localization, and trafficking in cellular and in vitro assay contexts. This approach is particularly useful when a stable, covalent dye attachment is preferred over noncovalent staining, and when downstream imaging workflows require consistent labeling density across samples.
2. Click-Constructed Fluorescent Probes
AF 568 alkyne is also used in fluorescent probe development, where an azide-functional recognition element (such as an affinity ligand, targeting moiety, or scaffold) is coupled to the AF 568 alkyne to produce a modular imaging reagent. In these workflows, the alkyne handle enables straightforward assembly of fluorescence-tagged constructs that can be evaluated in microscopy, plate-based fluorescence assays, or custom imaging pipelines. The resulting covalent dye conjugates are commonly employed to visualize molecular interactions, monitor reagent localization, or generate fluorescent tools for mechanistic studies in biological systems.
3. Polymer And Surface Functionalization
AF 568 alkyne supports fluorescence labeling of azide-functional polymers, hydrogels, and biomaterials, enabling researchers to fabricate fluorescently traceable materials for microscopy and materials characterization. By click-coupling the dye to azide-bearing surfaces or polymer networks, teams can generate stable fluorescent coatings or bulk-labeled materials used to study diffusion, transport, and material-biomolecule interactions. This application is especially relevant for biomaterials science workflows where fluorescent tagging must remain attached during washing, incubation, and imaging steps.
4. Flow Cytometry Labeling Reagents
AF 568 alkyne is used to prepare fluorescent conjugates for flow cytometry experiments when azide-functional targets are available, such as azide-modified antibodies, ligands, or labeling reagents. After click conjugation, the AF 568-labeled constructs can be used to quantify fluorescence associated with labeled targets in heterogeneous mixtures, supporting cell-sorting and population-level imaging readouts. This workflow is commonly selected when researchers need covalent dye attachment and reproducible labeling for multi-sample comparisons.
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