2-Ethynyl-ATP (2-EATP)

2-Ethynyl-adenosine-5’-triphosphate, Sodium salt

Catálogo Nº Apresentação Preço (R$) Comprar
CLK-NU-004S 100 μl (10 mM)Sob demanda Adicionar ao Carrinho
CLK-NU-004L 5 x 100 μl (10 mM)Sob demanda Adicionar ao Carrinho
Structural formula of 2-Ethynyl-ATP (2-EATP) (2-Ethynyl-adenosine-5’-triphosphate, Sodium salt)
Structural formula of 2-Ethynyl-ATP (2-EATP)

For general laboratory use.

Envio: shipped on gel packs

Condições de armazenamento: store at -20 °C
Short term exposure (up to 1 week cumulative) to ambient temperature possible.

Validade: 12 months after date of delivery

Fórmula molecular: C12H16N5O13P3

Peso molecular: 531.20 g/mol

Pureza: ≥ 90 % (HPLC), contains approx. 6 % 2-Ethynyl-ADP

Forma: solution in 100 mM Tris-HCl

Concentração: 10 mM - 11 mM

pH: 7.5 ±0.5

Propriedades espectroscópicas: λmax 265 nm, ε 10.6 L mmol-1 cm-1 (Tris-HCl pH 7.5)

Formulários:
in vitro polyadenylation of RNA[1]

Descrição:
2-Ethynyl-labeled adenosine triphosphate (2-EATP) is suitable for in vitro polyadenylation of RNA with recombinant poly(A) polymerase[1].

The resulting Alkyne-functionalized RNA can subsequently be processed via Cu(I)-catalyzed Azide-Alkyne click
chemistry (CUAAC) that offers the choice
to introduce a Biotin group for subsequent purification tasks (via Azides
of Biotin)to introduce fluorescent group for subsequent microscopic imaging (via
Azides of fluorescent dyes)to crosslink the RNA to azide-functionalized biomolecules e.g.proteins

Presolski et al.[2] and Hong et al.[3] provide a general protocol for Cu(I)-catalyzed click chemistry reactions that may be used as a starting point for the set up and optimization of individual assays.

Produtos relacionados:

  • 5-Ethynyl-adenosine (5-EA), #CLK-N005
  • Copper (II)-Sulphate (CuSO4), #CLK-MI004
  • Tris(3-hydroxypropyltriazolylmethyl)amine (THPTA), #CLK-1010
  • Sodium Ascorbate (Na-Ascorbate), #CLK-MI005

Referências selecionadas:
[1] Curanovic et al. (2013) Global profiling of stimulus-induced polyadenylation in cells using a poly (A) trap. Nat. Chem. Biol. 9:671.

[2] Presolski et al. (2011) Copper-Catalyzed Azide-Alkyne Click Chemistry for Bioconjugation. Current Protocols in Chemical Biology 3:153.

[3] Hong et al. (2011) Analysis and Optimization of Copper-Catalyzed Azide-Alkyne Cycloaddition for Bioconjugation. Angew. Chem. Int. Ed. 48:9879.