Sulfo-Cyanine3 azide
| Cat. # | Quantity | Price | Lead time | Buy this product |
|---|---|---|---|---|
| A1330 | 1 mg | $110.00 | in stock | |
| B1330 | 5 mg | $290.00 | in stock | |
| C1330 | 10 mg |
$470.00
|
in stock | |
| D1330 | 25 mg |
$690.00
|
in stock | |
| E1330 | 50 mg |
$1270.00
|
in stock | |
| F1330 | 100 mg |
$1990.00
|
in stock |
Sulfo-Cyanine3 azide is a water-soluble dye azide for Click Chemistry. Absorbance and emission of the dye are identical to Cy3® fluorophore.
Brightness and photostability of fluorophore, together with high water solubility, makes this reagent an ideal choice for Click chemistry labeling of various molecules in aqueous phase.
Click reaction can be carried out in pure water without need to use organic co-solvent. The reagent is designed for the labeling of sensitive molecules such as proteins, and even intact biological objects.
Sulfo-Cyanine3 absorbance and emission spectra
Recommended protocol
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An activated ester for the introduction of alkyne into peptides/proteins.Coumarin 343 X azide
Coumarin 343 is a blue emitting fluorophore that can serve as a FRET donor for fluorescein (FAM). This azide derivative can be conjugated with alkynes by Click chemistry. An extended linker arm between the fluorophore and the azide group enhances solubility, and provides spatial separation between the dye and the biomolecule.Cyanine3 alkyne
Cyanine3 alkyne is a fluorescent dye alkyne for Click Chemistry.General properties
| Appearance: | dark red crystals |
| Molecular weight: | 736.94 |
| CAS number: | 2055138-89-9 (sodium salt), 1658416-54-6 |
| Molecular formula: | C33H41N6KO7S2 |
| Solubility: | soluble in water (0.62 M = 46 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. |
| MSDS: | Download |
| Product specifications |
Spectral properties
| Excitation 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
- Wells, C.I.; Al-Ali, H.; Andrews, D.M.; Asquith, C.R.M.; Axtman, A.D.; Chung, M.; Dikic, I.; Ebner, D.; Elkins, J.M.; Ettmayer, P.; Fischer, C.; Frederiksen, M.; Gray, N.S.; Hatch, S.; Knapp, S.; Lee, S.; Lücking, U.; Michaelides, M.; Mills, C.E.; Müller, S.; Owen, D.; Picado, A.; Ramadan, K.; Saikatendu, K.S.; Schröder, M.; Stolz, A.; Tellechea, M.; Treiber, D.K.; Turunen, B.J.; Vilar, S.; Wang, J.; Zuercher, W.J.; Willson, T.M.; Drewry, D.H. The Kinase Chemogenomic Set (KCGS): An open science resource for kinase vulnerability identification. bioRxiv, preprint. doi: 10.1101/2019.12.22.886523
- Syga, L.; De Vries, R.H.; van Oosterhout, H.; Bartelds, R.; Boersma, A.J.; Roelfes, G.; Poolman, B. A trifunctional linker for palmitoylation and peptide and protein localization in biological membranes. ChemBioChem, in press. doi: 10.1002/cbic.201900655
- Li, Z.; Pinch, B.J.; Olson, C.M.; Donovan, K.A.; Nowak, R.P.; Mills, C.E.; Scott, D.A.; Doctor, Z.M.; Eleuteri, N.A.; Chung, M.; Sorger, P.K.; Fischer, E.S.; Gray, N.S. Development and Characterization of a Wee1 Kinase Degrader. Cell Chemical Biology, 2020, 27(1), 57–65.e9. doi: 10.1016/j.chembiol.2019.10.013
- Ereskovsky, A.V.; Tokina, D.B.; Saidov, D.M.; Baghdiguian, S.; Le Goff, E.; Lavrov, A.I. Transdifferentiation and mesenchymal-to-epithelial transition during regeneration in Demospongiae (Porifera). Journal of Experimental Zoology. Part B, 2020, 334(1), 37–58. doi: 10.1002/jez.b.22919
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