ROX azide, 5- isomer

ROX (Rhodamine X, Rhodamine 101) Azides Microscopy
Cat. # Quantity Price Lead time
11230 100 uL, 10 mM/DMSO $110.00 in stock
31230 500 uL, 10 mM/DMSO $210.00 in stock
41230 1 mL, 10 mM/DMSO $410.00 in stock
A1230 1 mg $110.00 in stock
B1230 5 mg $210.00 in stock
C1230 10 mg $310.00 in stock
D1230 25 mg $410.00 in stock
E1230 50 mg $695.00 in stock
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ROX (rhodamine-X) azide, solid material, and 10 mM solution in DMSO, labeling reagent for Click Chemistry. ROX is a red-emitting rhodamine dye possessing high brightness and fluorescence quantum yield.

Pure 5-isomer.

Can replace Alexa Fluor 568.

ROX azide, 5- isomer, D1230
ROX azide, 5- isomer, D1230
ROX azide, 5- isomer, x1230
ROX azide, 5- isomer, 10 mM/DMSO, 41230
ROX azide, 5- isomer, 10 mM/DMSO, 41230
ROX azide, 5- isomer, 10 mM/DMSO, 41230
ROX azide, 5- isomer, 10 mM/DMSO, x1230
Structure of ROX azide, 5-isomer
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Absorption and emission spectra of ROX dye

Absorption and emission spectra of ROX dye

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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.

General properties

Appearance: dark crimson powder / red solution
Molecular weight: 616.71
Molecular formula: C36H36N6O4
Solubility: good in polar organic solvents (DMF, DMSO, alcohols), low in water
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: 570
ε, L⋅mol−1⋅cm−1: 93000
Emission maximum, nm: 591
Fluorescence quantum yield: 1.0

Product citations

  1. Feltes, M.; Moores, S.; Gale, S.E.; Krishnan, K.; Mydock-McGrane, L.; Covey, D.F.; Ory, D.S.; Schaffer, J.E. Synthesis and characterization of diazirine alkyne probes for the study of intracellular cholesterol trafficking. Journal of Lipid Research, 2019, 60(3), 707–716. doi: 10.1194/jlr.D091470
  2. Verardi, R.; Kim, J.-S.; Ghirlando, R.; Banerjee, A. Structural Basis for Substrate Recognition by the Ankyrin Repeat Domain of Human DHHC17 Palmitoyltransferase. Structure, 2017, 25(9), 1337–1347. doi: 10.1016/j.str.2017.06.018
  3. Bak, D.W.; Pizzagalli, M.D.; Weerapana, E. Identifying Functional Cysteine Residues in the Mitochondria. ACS Chemical Biology, 2017, 12(4), 947–957. doi: 10.1021/acschembio.6b01074
  4. Nåbo, L.J.; Madsen, C.S.; Jensen, K.J.; Kongsted, J.; Astakhova, K. Ultramild Protein-Mediated Click Chemistry Creates Efficient Oligonucleotide Probes for Targeting and Detecting Nucleic Acids. ChemBioChem, 2015, 16(8), 1163–1167. doi: 10.1002/cbic.201500145
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