TAMRA azide, 5-isomer
Cat. # | Quantity | Price | Lead time | Buy this product |
---|---|---|---|---|
A7130 | 1 mg | $110 | in stock | |
B7130 | 5 mg | $135 | in stock | |
C7130 | 10 mg | $210 | in stock | |
D7130 | 25 mg | $390 | in stock | |
E7130 | 50 mg | $595 | in stock | |
F7130 | 100 mg | $790 | in stock |
TAMRA (TMR, tetramethylrhodamine) azide, solid compound, and 10 mM solution in DMSO, labeling reagent for click chemistry. Pure 5-isomer. TAMRA is often used as a FRET acceptor for FAM fluorophore. Can replace DyLight 549.
Absorption and emission spectra of 5-TAMRA
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sulfo-Cyanine5 DBCO
Water-soluble cycloalkyne for copper-free click chemistry reaction with azides. A derivative of sulfo-Cyanine5.Thiazole Orange NHS ester
Thiazole Orange NHS ester for labeling biomolecules (peptides, proteins, amino-DNA, etc.). Thiazole orange is a cyanine dye that is essentially dark in solution but has a bright fluorescence in double-stranded DNA and RNA.ROX azide, 5-isomer
Azide derivative of ROX (Rhodamine X, Rhodamine 101) dye for biomolecule labeling via click chemistry. Pure 5-isomer.General properties
Appearance: | violet solid / solution |
Mass spec M+ increment: | 512.2 |
Molecular weight: | 512.56 |
CAS number: | 825651-66-9 |
Molecular formula: | C28H28N6O4 |
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/absorption maximum, nm: | 541 |
ε, L⋅mol−1⋅cm−1: | 84000 |
Emission maximum, nm: | 567 |
Fluorescence quantum yield: | 0.1 |
CF260: | 0.32 |
CF280: | 0.19 |
Product citations
- Yu, T.; Hou, D.; Zhao, J.; Lu, X.; Greentree, W.K.; Zhao, Q.; Yang, M.; Conde, D.-G.; Linder, M.E.; Lin, H. NLRP3 Cys126 palmitoylation by ZDHHC7 promotes inflammasome activation. Cell reports, 2024, 43(4), 114070. doi: 10.1016/j.celrep.2024.114070
- Reddi, R. N.; Rogel, A.; Gabizon, R.; Rawale, D. G.; Harish, B.; Marom, S.; Tivon, B.; Arbel, Y. S.; Gurwicz, N.; Oren, R.; David, K.; Liu, J.; Duberstein, S.; Itkin, M.; Malitsky, S.; Barr, H.; Katz, B.-Z.; Herishanu, Y.; Shachar, I.; Shulman, Z.; London, N. Sulfamate Acetamides as Self-Immolative Electrophiles for Covalent Ligand-Directed Release Chemistry. J. Am. Chem. Soc, 2023, 145(6), 3346–3360. doi: 10.1021/jacs.2c08853
- Komaniecki, G.; Camarena, M. D. C.; Gelsleichter, E.; Mendoza, R.; Subler, M.; Windle, J. J.; Dozmorov, M. G.; Lai, Z.; Sarkar, D.; Lin, H. Astrocyte Elevated Gene-1 Cys75 S-Palmitoylation by ZDHHC6 Regulates Its Biological Activity. Biochemistry, 2023, 62(2), 543–553. doi: 10.1021/acs.biochem.2c00583
- Hulce, K.R.; Jaishankar, P.; Lee, G.M.; Bohn, M.-F.; Connelly, E.J.; Wucherer, K.; Ongpipattanakul, C.; Volk, R.F.; Chuo, S.-W.; Arkin, M.R.; Renslo, A.R.; Craik, C.S. Inhibiting a dynamic viral protease by targeting a non-catalytic cysteine. Cell Chemical Biology, 2022, 29(5), 785-798.e19. doi: 10.1016/j.chembiol.2022.03.007
Product is offered and sold for research purposes only. Product is not tested for safety and efficacy in food, drug, medical device, cosmetic, no express or implied authorization to use for any other purpose, including, without limitation, in vitro diagnostic purposes, for humans or animals or for commercial purposes.
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