sulfo-Cyanine3 amine
| Cat. # | Quantity | Price | Lead time | Buy this product |
|---|---|---|---|---|
| 113C0 | 1 mg | $115 | in stock | |
| 213C0 | 5 mg | $285 | in stock | |
| 413C0 | 25 mg |
$680
|
in stock | |
| 513C0 | 50 mg |
$1270
|
in stock | |
| 613C0 | 100 mg |
$1990
|
in stock |
A water-soluble dye with an amino group that is useful for the conjugation with electrophiles and for enzymatic transamination labeling.
sulfo-Cyanine3 is a sulfonated analog of Cy3®, which is compatible with various fluorescence measuring equipment. The dye is highly photostable. It is also easily detectable by the naked eye.
Sulfo-Cy3 absorbance and emission spectra
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Water soluble sulfo-Cyanine3 SE activated ester for amino-biomolecule labeling.BDP TMR amine
BDP TMR amine is an amino dye for TAMRA channel. The dye possesses bright fluorescence and is well suitable for the fluorescence polarization assays.
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General properties
| Appearance: | dark red solid |
| Molecular weight: | 714.94 |
| CAS number: | 2183440-43-7 |
| Molecular formula: | C36H50N4O7S2 |
| IUPAC name: | 3H-Indolium, 1-[6-[(6-aminohexyl)amino]-6-oxohexyl]-2-[3-(1,3-dihydro-1,3,3-trimethyl-5-sulfo-2H-indol-2-ylidene)-1-propen-1-yl]-3,3-dimethyl-5-sulfo-, inner salt |
| Solubility: | well soluble in water (0.49 M = 350 g/L), alcohols, DMSO, DMF |
| 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
- Henry, W.S.; Müller, S.; Yang, J.-S.; Innes-Gold, S.; Das, S.; Reinhardt, F.; Sigmund, K.; Phadnis, V.V.; Wan, Z.; Eaton, E.; Sampaio, J.L.; Bell, G.W.; Viravalli, A.; Hammond, P.T.; Kamm, R.D.; Cohen, A.E.; Boehnke, N.; Hsu, V.W.; Levental, K.R.; Rodriguez, R.; Weinberg, R.A. Ether lipids influence cancer cell fate by modulating iron uptake. bioRxiv, 2024, preprint. doi: 10.1101/2024.03.20.585922
- Bos, I.; Timmerman, M.; Sprakel, J. FRET-Based Determination of the Exchange Dynamics of Complex Coacervate Core Micelles. Macromolecules, 2021, 54(1), 398–411. doi: 10.1021/acs.macromol.0c02387
- Zhang, Q.; Scigliano, A.; Biver, T.; Pucci, A.; Swager, T.M. Interfacial Bioconjugation on Emulsion Droplet for Biosensors. Bioorganic & Medicinal Chemistry, 2018, 26(19), 5307–5313. doi: 10.1016/j.bmc.2018.04.020
- Sobotzki, N.; Schafroth, M.A.; Rudnicka, A.; Koetemann, A.; Marty, F.; Goetze, S.; Yamauchi, Y.; Carreira, E.M.; Wollscheid, B. HATRIC-based identification of receptors for orphan ligands. Nature Communications, 2018, 9, 1519. doi: 10.1038/s41467-018-03936-z
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