
Sulfo-Cyanine5.5 amine | CAS 2183440-45-9
| Catalog Number | F03-0009 |
| Category | sulfo-Cyanine5.5 |
| Molecular Formula | C46H54K2N4O13S4 |
| Molecular Weight | 1077.41 |
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Product Introduction
Sulfo-Cyanine5.5 is a water soluble cyanine dye for far red / NIR applications such as in vivo imaging. The dye possesses four sulfonate groups that render it highly hydrophilic and water soluble. As well as other cyanines, sulfo-Cyanine5.5 has an outstanding extinction coefficient that makes it a bright fluorescent label for the far red region. This is an amine-containing fluorescent dye. The amine group is separated from the fluorophore by a relatively long linker that facilitates conjugation. The aliphatic primary amine group can be coupled with various electrophiles (activated esters, epoxides, etc), and also be used in enzymatic transamination labeling.
Chemical Information
Product Specification
Application
Chemical Information
| Related CAS | 2183440-46-0 (potassium salt) |
| Purity | NMR 1H, HPLC-MS (95%) |
| Solubility | good in water, DMF, DMSO |
| Appearance | dark blue solid |
Product Specification
| ε, L⋅mol-1⋅cm-1 | 235000 |
| Excitation | 673 |
| Emission | 691 |
| 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
Sulfo-Cyanine5.5 amine is a sulfonated cyanine dye featuring an amine-reactive handle for fluorescent labeling workflows, enabling water-compatible conjugation with biomolecules and polymers. Its far-red emission supports low-background imaging and fluorescence readouts in microscopy and fluorescence-based assays, where stable labeling of proteins, peptides, and nucleic-acid-containing constructs is required. In practice, the sulfonate functionality helps maintain aqueous solubility and reduces nonspecific hydrophobic interactions during labeling and subsequent handling.
1. Protein Conjugation Labeling
Sulfo-Cyanine5.5 amine is commonly used by protein chemistry and chemical biology groups to generate far-red fluorescent protein conjugates for imaging and quantitative fluorescence assays. Researchers typically incorporate the dye into antibodies, antibody fragments, enzymes, and affinity reagents to visualize binding events, track biomolecule localization, or monitor reaction progress in fluorescence readouts. The sulfonated dye scaffold supports aqueous labeling conditions and helps maintain labeling performance during buffer exchanges and downstream assay steps, making it practical for workflows that require reproducible dye loading and consistent fluorescence intensity.
2. Fluorescence Microscopy Tracing
Sulfo-Cyanine5.5 amine supports cellular and subcellular fluorescence microscopy applications where far-red excitation/emission improves contrast against cellular autofluorescence. Imaging teams use dye-labeled proteins, peptides, and polymer carriers to trace biomolecule uptake, trafficking, and surface association in fixed-cell and imaging-compatible preparations. The amine-reactive dye format is also used to prepare fluorescent standards and labeled controls that align with common far-red filter sets, enabling consistent visualization across experiments such as co-localization studies and multi-channel imaging panels.
3. Flow Cytometry Staining
Sulfo-Cyanine5.5 amine is frequently selected for flow cytometry staining strategies that rely on far-red fluorescence to reduce spectral overlap with common fluorophores. Flow cytometry users generate dye-labeled antibodies or labeling reagents to quantify binding to cell-surface targets or to track labeled biomolecules in cell-associated assays. The sulfonated cyanine structure helps support aqueous labeling and washing steps typical of cytometry workflows, supporting robust signal retention during sample processing and instrument acquisition.
4. Nucleic Acid Conjugate Preparation
Sulfo-Cyanine5.5 amine is used in nucleic-acid analysis workflows to produce fluorescently labeled oligonucleotide conjugates for imaging and fluorescence-based nucleic-acid assays. Researchers incorporate the dye into nucleic-acid-containing constructs through amine-directed labeling of modified biomolecules or nucleic-acid-associated carriers, enabling visualization of hybridization-related workflows and fluorescent tracking of nucleic-acid assemblies. Far-red emission from the cyanine scaffold is particularly useful when nucleic-acid assays are performed alongside other fluorescent channels or when background from biological matrices needs to be minimized.
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