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Product Introduction
Cyanine2 minimal dye for protein labeling, an equivalent of Cy2® NHS ester minimal dye. This reagent is specially quantified-each package contains specified amount of NHS ester with quantity variation within 10%.
Chemical Information
Product Specification
Application
Chemical Information
| Purity | NMR 1H, HPLC-MS, functional testing |
| Appearance | yellow solid |
Product Specification
| Excitation | 490 |
| Emission | 510 |
| Storage | 12 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
Cyanine2 NHS ester minimal dye is a fluorescent cyanine dye designed for NHS ester–based bioconjugation, enabling covalent attachment to primary amine groups on proteins, peptides, and other amine-bearing biomolecules. As a compact, bright labeling scaffold commonly used in fluorescence-based molecular imaging workflows, it is frequently selected when researchers need stable dye conjugates with streamlined conjugation chemistry. Its dye structure supports sensitive optical readouts in microscopy, flow cytometry, and assay development, making it a practical reagent for building labeled reagents and imaging probes.
1. Protein Labeling For Imaging
Cyanine2 NHS ester minimal dye is widely used to generate fluorescent protein conjugates for cellular and molecular imaging experiments, where covalent attachment to lysine residues or N-terminal amines provides robust, well-defined labeling. Researchers commonly employ this dye to prepare labeled antibodies, enzyme reporters, and binding proteins used as imaging reagents in microscopy and related fluorescence workflows. The NHS ester handle is particularly valued in labeling pipelines that require rapid coupling under standard bioconjugation conditions, producing dye-protein constructs suitable for tracking biomolecular localization and distribution in complex samples.
2. Antibody Conjugates For Assays
Cyanine2 NHS ester minimal dye is a common choice for preparing antibody conjugates used in immunoassays and fluorescence-based binding studies, including assay development in diagnostic reagent research and industrial assay prototyping. By targeting accessible primary amines on antibody surfaces, the dye enables stable fluorescent tagging that supports readout by plate readers and fluorescence imaging systems. This reagent is also used to create labeled secondary reagents and antibody-derived constructs for multiplexing strategies where consistent dye conjugation is important for comparing signals across targets.
3. Peptide And Ligand Tagging
Cyanine2 NHS ester minimal dye is used to label peptides and small ligands that contain primary amines, supporting the creation of fluorescent targeting tools for biochemical characterization and molecular interaction studies. In chemical biology workflows, the dye conjugate format is often selected to visualize binding events, monitor reagent uptake or association, and generate fluorescent standards for assay calibration. The minimal dye format helps maintain the functional properties of the labeled ligand while providing a strong fluorescence signal for downstream imaging or detection platforms.
4. Surface And Material Functionalization
Cyanine2 NHS ester minimal dye is applied in biomaterials science and surface chemistry to fluorescently functionalize amine-containing polymers, beads, and membrane surfaces for imaging and materials characterization. Researchers use the NHS ester reactivity to immobilize the dye onto substrates that present primary amines, enabling visualization of coatings, tracking of surface-bound components, and development of fluorescent labeling strategies for assay formats. This approach is also used to produce labeled solid supports for workflow development, including studies that require stable surface fluorescence over repeated handling and measurement steps.
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