
sulfo-Cyanine3 tyramide
| Catalog Number | F03-0034 |
| Category | sulfo-Cyanine3 |
| Molecular Formula | C38H44KN3O8S2 |
| Molecular Weight | 774.02 |
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Product Introduction
sulfo-Cyanine3 tyramide is a component of many tyramide signal amplification (TSA) kits. It can be used with any antibody or other molecules (streptavidin, etc.) conjugated to HRP to stain cells and tissues by immunofluorescence methods.
Chemical Information
Product Specification
Application
Chemical Information
| Solubility | Soluble in water, DMF, DMSO |
| Appearance | Red Powder |
Product Specification
| Excitation | 548 |
| Emission | 563 |
Application
Sulfo-Cyanine3 tyramide is a cyanine-based tyramide labeling reagent designed for covalent fluorescence tagging in fixed or permeabilized biological samples. Its sulfonated, water-soluble character supports use in aqueous staining workflows, while the reactive tyramide functionality enables retention of the fluorescent signal at the labeling site after enzymatic activation. In fluorescence microscopy and immunostaining development, this reagent is commonly used to amplify and localize target-associated fluorescence with cyanine emission in the red-orange spectral region.
1. Immunofluorescence Signal Amplification
Sulfo-Cyanine3 tyramide is widely used in immunofluorescence workflows where enzymatic activation (commonly peroxidase-based detection systems) is used to deposit a covalently bound cyanine label near the antibody binding site. Researchers and diagnostic-reagent developers use it to increase the visibility of low-abundance targets in fixed cell preparations and tissue sections, where retained, covalent labeling helps maintain spatial localization during washing and imaging. The sulfonated dye design supports staining in standard aqueous buffer systems used with antibody panels and secondary detection reagents, making it a practical choice for multiplex staining strategies that rely on robust post-wash signal retention.
2. Fluorescence Microscopy Localization
Sulfo-Cyanine3 tyramide supports high-contrast cellular and subcellular localization studies by providing covalent fluorescence that remains associated with the labeled structures after fixation and extensive wash steps. Microscopy users apply it in workflows that require durable staining for quantitative imaging, co-localization experiments, and time-intensive image acquisition, including studies of protein distribution in cultured cells and labeled targets in permeabilized samples. Because the cyanine fluorophore is compatible with common red/orange fluorescence channels, it integrates into established laser and filter sets for confocal and widefield microscopy used in cell biology and biomaterials research.
3. Multiplex Tyramide Staining Panels
Sulfo-Cyanine3 tyramide is frequently incorporated into multiplex immunostaining panel development where covalent deposition chemistry helps reduce signal loss between sequential staining and imaging cycles. Assay developers use it to build multi-target workflows with spectrally separated dyes, leveraging the tyramide approach to generate strong, retained signals from each detection step. In practice, this enables researchers to map multiple biomarkers within the same sample while maintaining consistent staining behavior across targets, which is especially valuable for comparative studies in fixed tissues and high-content microscopy experiments.
4. Flow Cytometry After Fixation
Sulfo-Cyanine3 tyramide can be used in flow cytometry workflows that rely on covalent labeling after fixation and enzymatic activation to improve retention of the fluorescent signal during washing and instrument analysis. Researchers use it when they need stable, wash-resistant fluorescence for quantifying labeled targets on fixed/permeabilized cells, such as in antibody-based profiling experiments and assay development for cellular biomarker panels. The water-soluble sulfonated dye format supports aqueous handling during staining and post-stain processing, aligning with typical sample preparation steps used prior to data acquisition.
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