sulfo-Cyanine3 DBCO
| Cat. # | Quantity | Price | Lead time | Buy this product |
|---|---|---|---|---|
| 113F0 | 1 mg | $110.00 | in stock | |
| 213F0 | 5 mg | $290.00 | in stock | |
| 413F0 | 25 mg |
$690.00
|
in stock | |
| 513F0 | 50 mg |
$1270.00
|
in stock | |
| 613F0 | 100 mg |
$1990.00
|
in stock |
Sulfo-Cyanine3 DBCO is a water soluble fluorescent dye with cycloalkyne group for copper free Click chemistry.
DBCO (dibenzocyclooctyne) is a cyclooctyne with very high reactivity towards azides, still possessing good stability.
Absorption and emission spectra of sulfo-Cyanine3
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Sulfo-Cyanine3 alkyne
A water soluble dye alkyne for copper-catalyzed Click Chemistry. The fluorophore Sulfo-Cyanine3 is a bright and photostable dye for the Cy3® channel.Sulfo-Cyanine5.5 alkyne
Alkyne functionalized, water soluble far red/near infrared emitting fluorophore sulfo-Cyanine5.5.Azidobutyric acid NHS ester
Activated ester for azido labeling of peptides and proteins.General properties
| Appearance: | red solid |
| Mass spec M+ increment: | 916.4 |
| Molecular weight: | 955.23 |
| Molecular formula: | C51H55N4KO8S2 |
| Solubility: | soluble in water (0.11 M = 11 g/L), DMF, DMSO |
| Quality control: | NMR 1H, HPLC-MS (95%) |
| Storage conditions: | 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. |
| MSDS: | Download |
| Product specifications |
Spectral properties
| Excitation/absorption maximum, nm: | 548 |
| ε, L⋅mol−1⋅cm−1: | 162000 |
| Emission maximum, nm: | 563 |
| Fluorescence quantum yield: | 0.1 |
| CF260: | 0.03 |
| CF280: | 0.06 |
Product citations
- Tugel, U.; Casas, M.G.; Wiltschi, B. Site-Specific Incorporation of Non-canonical Amino Acids by Amber Stop Codon Suppression in Escherichia coli. Peptide and Protein Engineering (Springer Protocols Handbooks), 2020, 267–281. doi: 10.1007/978-1-0716-0720-6_14
- Desai, B.J.; Gonzalez, R.L. Multiplexed genomic encoding of non-canonical amino acids for labeling large complexes. Nature Chemical Biology, 2020, 16, 1129–1135. doi: 10.1038/s41589-020-0599-5
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