
AF 568 carboxylic acid
| Catalog Number | R01-0460 |
| Category | Alexa Fluor |
| Molecular Formula | C33H28K2N2O11S2 |
| Molecular Weight | 770.91 |
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Product Introduction
AF 568 is a fluorescent dye with excitation maximum at 572 nm and emission maximum at 598 nm. This dye has better photostability than traditional fluorescent stains (fluorescein isothiocyanate FITC, phycoerythrin PE etc.).
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | BP Fluor 568 carboxylic acid |
| IUPAC Name | dipotassium;[13-(2,5-dicarboxyphenyl)-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=CC(=C6)C(=O)O)C(=O)O)CS(=O)(=O)[O-])(C)C)CS(=O)(=O)[O-])C.[K+].[K+] |
| InChI | InChI=1S/C33H30N2O11S2.2K/c1-32(2)12-17(14-47(40,41)42)20-8-23-27(10-25(20)34-32)46-28-11-26-21(18(15-48(43,44)45)13-33(3,4)35-26)9-24(28)29(23)22-7-16(30(36)37)5-6-19(22)31(38)39;;/h5-13,34H,14-15H2,1-4H3,(H,36,37)(H,38,39)(H,40,41,42)(H,43,44,45);;/q;2*+1/p-2 |
| InChIKey | ULPHFJDFCQUIAD-UHFFFAOYSA-L |
| Solubility | Soluble in water, DMSO and DMF |
| Appearance | Violet Solid |
Product Specification
| Excitation | 572 |
| Emission | 598 |
Application
AF 568 carboxylic acid is a red-emitting fluorophore building block commonly used to prepare fluorescent labeling reagents and conjugates for microscopy and fluorescence-based assays. As a carboxylic acid derivative, it is typically employed for covalent attachment to amine-containing biomolecules or polymers, enabling stable tracking of proteins, peptides, and other targets in labeling workflows. Its bright visible emission profile supports routine fluorescence imaging and assay development on standard fluorescence instrumentation.
1. Protein And Antibody Labeling
AF 568 carboxylic acid is used by researchers to generate AF 568-labeled proteins, antibodies, and antibody fragments for fluorescence microscopy and immunoassay development. In typical workflows, the dye is incorporated into labeling conjugates that retain binding or recognition behavior of the biomolecule while providing a red fluorescent readout for target localization, binding studies, and quantitative fluorescence measurements. This reagent format is especially useful when a carboxyl-functional fluorophore is preferred for downstream conjugation chemistry to amine-bearing biomolecules.
2. Fluorescence Microscopy Tracing
AF 568 carboxylic acid supports cellular and biomaterial imaging applications where red fluorescence labeling is required to visualize distribution, trafficking, or association of labeled components. Lab groups use AF 568 conjugates to track biomolecules in fixed-cell experiments, to label extracellular or surface-associated targets on engineered materials, and to create multicolor imaging panels when paired with spectrally compatible dyes. The dye's visible emission makes it straightforward to integrate into common widefield and confocal microscopy workflows with standard filter sets.
3. Flow Cytometry Labeling
AF 568 carboxylic acid is applied in flow cytometry reagent development to produce fluorescent conjugates for cell-surface or intracellular labeling experiments that rely on red emission detection. Scientists use AF 568-labeled antibodies, affinity reagents, or other amine-reactive conjugates to quantify fluorescence intensity by population, enabling characterization of binding, uptake, or marker expression in assay development and analytical studies. This labeling approach is frequently used in method development for panel design where consistent red-channel signal is required.
4. Fluorescence Bioassay Reagents
AF 568 carboxylic acid is also used to construct fluorescent assay reagents, including labeled binding partners for fluorescence-based readouts and calibration standards for assay workflows. In biochemical and chemical biology studies, AF 568 conjugates can be incorporated into binding assays, labeling-based detection formats, and fluorescence quantification experiments where a stable red fluorophore signal is advantageous. Researchers often select this dye building block when they need a covalently attachable fluorophore to generate reproducible fluorescent reagents for routine plate-based or cuvette-based measurements.
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