2'/3'-O-Anthraniloyl-guanosine-5'-triphosphate, Triethylammonium salt
| Cat. No. | Amount | Price (EUR) | Buy / Note |
|---|---|---|---|
| NU-230S | 150 μl (10 mM) | 150,10 | Add to Basket/Quote Add to Notepad |
| NU-230L | 5 x 150 μl (10 mM) | 439,50 | Add to Basket/Quote Add to Notepad |
For general laboratory use.
Shipping: shipped on gel packs
Storage Conditions: store at -20 °C
Short term exposure (up to 1 week cumulative) to ambient temperature possible.
Shelf Life: 12 months after date of delivery
Molecular Formula: C17H21N6O15P3 (free acid)
Molecular Weight: 642.30 g/mol (free acid)
Exact Mass: 642.03 g/mol (free acid)
CAS#: 85287-50-9 (3'-isomer)
Purity: ≥ 95 % (HPLC)
Form: solution in water
Color: colorless to slightly yellow
Concentration: 10 mM - 11 mM
pH: 7.5 ±0.5
Spectroscopic Properties: λmax 258/332 nm, ε 9.8/4.6 L mmol-1 cm-1 (Tris-HCl pH 7.5), λexc 332 nm, λem 423 nm
BIOZ Product Citations:
Selected References:
Gunawardana et al. (2015) Efficient preparation and properties of mRNAs containing a fluorescent cap analog: Anthraniloyl-m7GpppG Translation (Austin). 3 (1):e988538.
Pinto et al. (2011) Structure-activity relationships for the interactions of 2'- and 3'- (O)- (N-methyl)anthraniloyl-substituted purine and pyrimidine nucleotides with mammalian adenylyl cyclases. Biochem. Pharmacol. 82 (4):358.
Taha et al. (2009) Molecular Analysis of the Interaction of Anthrax Adenylyl Cyclase Toxin, Edema Factor, with 2 (3)-O- (N- (methyl)anthraniloyl)-Substituted Purine and Pyrimidine Nucleotides. Molecular Pharmacology 75 (3):693.
Goettle et al. (2007) Molecular analysis of the interaction of Bordetella pertussis adenylyl cyclase with fluorescent nucleotides. Molecular Pharmacology 72 (3):526.
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