sulfo-Cyanine3.5 NHS ester
| Cat. # | Quantity | Price | Lead time | Buy this product |
|---|---|---|---|---|
| 12320 | 1 mg | $125 | in stock | |
| 22320 | 5 mg | $325 | in stock | |
| 42320 | 25 mg |
$850
|
in stock | |
| 52320 | 50 mg |
$1490
|
in stock | |
| 62320 | 100 mg |
$1990
|
in stock |
Cyanine3.5 is a fluorescent dye with absorption and emission intermediate between Cyanine3 and Cyanine5. The sulfonated version contains four sulfo groups, which ensure high solubility and hydrophilicity of the fluorophore and labeled conjugates.
The NHS ester reactive group allows labeling of primary and secondary amine groups.
Absorption and emission spectra of sulfo-Cyanine3.5
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sulfo-Cyanine5.5 azide
sulfo-Cyanine5.5 azide is a derivative of water-soluble far-red emitting fluorescent cyanine dye. The azide group can be conjugated by either copper-catalyzed or copper-free click chemistry with alkynes and cycloalkynes.EDC (N-ethyl-N'-(3-dimethylaminopropyl)carbodiimide), coupling grade
Water soluble carbodiimide for the coupling of carboxylic acids with amines.TR-X-NHS ester, 5-isomer
TR is a red-emitting fluorescent dye based on sulforhodamine scaffold, an amine-reactive NHS ester.
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General properties
| Appearance: | deep purple powder |
| Molecular weight: | 1088.33 |
| CAS number: | 2231670-91-8 (without cation) |
| Molecular formula: | C42H40N3K3O16S4 |
| Solubility: | good in water, DMF, DMSO |
| Quality control: | NMR 1H, HPLC-MS (95%) |
| Storage conditions: | Storage: 12 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: | 576 |
| ε, L⋅mol−1⋅cm−1: | 139000 |
| Emission maximum, nm: | 603 |
| Fluorescence quantum yield: | 0.11 |
| CF260: | 0.16 |
| CF280: | 0.17 |
Product citations
- McGuire, K.; He, S.; Gracie, J.; Bryson, C.; Zheng, D.; Clark, A.W.; Koehnke, J.; France, D.J.; Nau, W.M.; Lee, T.-C.; Peveler, W.J. Supramolecular Click Chemistry for Surface Modification of Quantum Dots Mediated by Cucurbit[7]uril. ACS nano, 2023, 17(21), 21585-21594. doi: 10.1021/acsnano.3c06601
- Shramova, E.; Proshkina, G.; Shipunova, V.; Ryabova, A.; Kamyshinsky, R.; Konevega, A.; Schulga, A.; Konovalova, E.; Telegin, G.; Deyev, S. Dual Targeting of Cancer Cells with DARPin-Based Toxins for Overcoming Tumor Escape. Cancers, 2020, 12(10), 3014. doi: 10.3390/cancers12103014
This Product is offered and sold for research purposes only. It has not been tested for safety and efficacy in food, drug, medical device, cosmetic, commercial or any other use. Supply does not express or imply authorization to use for any other purpose, including, without limitation, in vitro diagnostic purposes, in the manufacture of food or pharmaceutical products, in medical devices or in cosmetic products.
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