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Principaux documents

A2767

Sigma-Aldrich

Adenosine 5′-triphosphate–Agarose

lyophilized powder

Synonyme(s) :

5′-ATP agarose

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About This Item

Numéro MDL:
Code UNSPSC :
41106500
eCl@ss :
32160414
Nomenclature NACRES :
NA.56

Source biologique

plant (Sea weed)

Niveau de qualité

Forme

lyophilized powder

Ampleur du marquage

1-5 μmol per mL

Matrice

cross-linked 4% beaded agarose

Activation de la matrice

cyanogen bromide

Fixation de matrice

C-8

Espaceur de matrice

9 atoms

Température de stockage

−20°C

Chaîne SMILES 

[X]Nc1ncnc2[n](cnc21)[C@@H]3O[C@@H]([C@H]([C@H]3O)O)CO[P](=O)(O[P](=O)(O[P](=O)(O)O)O)O

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Catégories apparentées

Description générale

Adenosine 5′-triphosphate–Agarose (5′-ATP-agarose) is a conjugate of 5′-ATP to crosslinked 4% beaded agarose (activated by cyanogen bromide), via the C-8 atom of 5′-ATP. 5′-ATP–agarose is applicable for affinity purification of various proteins and enzymes like cyclin-dependent kinase 2 (CDK2), heat shock proteins, and cryptochromes.

Application

Adenosine 5′-triphosphate Agarose (5′-ATP agarose) has been used in affinity chromatography to purify uridine kinase from Ehrlich ascites tumor cells.
Adenosine 5′-triphosphate–Agarose (5′-ATP–agarose) is applicable for affinity purification of various proteins and enzymes like cyclin-dependent kinase 2 (CDK2), heat shock proteins-70 (HSP-70), and cryptochromes. 5′-ATP agarose has been used in affinity chromatography to purify uridine kinase from Ehrlich ascites tumor cells.

Forme physique

Lyophilized powder stabilized with lactose

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


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Consulter la Bibliothèque de documents

C Prodromou et al.
The EMBO journal, 18(3), 754-762 (1999-02-02)
The in vivo function of the heat shock protein 90 (Hsp90) molecular chaperone is dependent on the binding and hydrolysis of ATP, and on interactions with a variety of co-chaperones containing tetratricopeptide repeat (TPR) domains. We have now analysed the
M Brungs et al.
Proceedings of the National Academy of Sciences of the United States of America, 92(1), 107-111 (1995-01-03)
5-Lipoxygenase (5-LO; EC 1.13.11.34) activity in the human monocytic cell line Mono Mac 6 was upregulated by combined treatment with transforming growth factor beta 1 (TGF-beta) and 1,25-dihydroxyvitamin D3 (VD3). In undifferentiated cells, 5-LO enzyme activity was undetectable. After the
L Fischer et al.
British journal of pharmacology, 152(4), 471-480 (2007-08-21)
Licofelone is a dual inhibitor of the cyclooxygenase and 5-lipoxygenase (5-LO) pathway, and has been developed for the treatment of inflammatory diseases. Here, we investigated the molecular mechanisms underlying the inhibition by licofelone of the formation of 5-LO products. The
Christian Feisst et al.
The Journal of pharmacology and experimental therapeutics, 315(1), 389-396 (2005-07-15)
Myrtucommulone (MC) and semimyrtucommulone (S-MC) are unique oligomeric, nonprenylated acylphloroglucinols contained in the leaves of myrtle (Myrtus communis). Although extracts of myrtle have been traditionally used in folk medicine for the treatment of various disorders, studies addressing select cellular or
F Geller et al.
Journal of ethnopharmacology, 128(3), 561-566 (2010-02-13)
Preparation from leaves of Cordia americana have been widely used in traditional medicine in South Brazil to treat wounds and various inflammations. The objective of this work was to identify the effective compounds in the ethanolic extract prepared from the

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