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G3907

Millipore

Agarose−glutathion

set of 3 pre-packed columns (2.5 ml each), (1:1 suspension in a 0.5 M NaCl + 20% ethanol solution)

Synonyme(s) :

Agarose glutathion à liaison S, Agarose-GSH

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About This Item

Numéro MDL:
Code UNSPSC :
41106500
Nomenclature NACRES :
NA.56

Niveau de qualité

Forme

(1:1 suspension in a 0.5 M NaCl + 20% ethanol solution)

Classe(s) chimique(s) de l'analyte

proteins (GST)

Conditionnement

set of 3 pre-packed columns (2.5 ml each)

Technique(s)

immunoprecipitation (IP): suitable
protein purification: suitable

Matrice

cross-linked 4% beaded agarose

Température de stockage

2-8°C

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Description générale

The resin in these columns consists of glutathione attached through the sulfur to epoxy activated, 4% cross-linked beaded agarose resulting in a 12 atom spacer.

Application

Affinity chromatography using glutathione-agarose permits rapid, mild, non-denaturing and highly selective purification of glutathione binding enzymes such as glutathione-S-transferase, glutathione peroxidase, and glyoxalase I.
The product was used in the design, synthesis and biological evaluation of new tryptamine and tetrahydro-β-carboline-based selective inhibitors of CDK4. It was also used to study Fascaplysin-inspired diindolyls as selective inhibitors of CDK4/cyclin D1.
La chromatographie d'affinité avec de l′agarose-glutathion assure une purification rapide, non dénaturante, en conditions douces et hautement sélective des protéines contenant des séquences de liaison au glutathion, telles que la glutathion S-transférase (GST), la glutathion peroxydase et la glyoxalase I.

Liaison

Suspension of Product No. G 4510

Forme physique

1:1 suspension in a 0.5 M NaCl + 20% ethanol solutionl

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

180.1 °F

Point d'éclair (°C)

82.3 °C


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Les clients ont également consulté

Paul R Jenkins et al.
Bioorganic & medicinal chemistry, 16(16), 7728-7739 (2008-07-25)
We present the design, synthesis and biological activity of a library of substituted (biphenylcarbonyl)-tryptamine and (biphenylcarbonyl)-tetrahydro-beta-carboline compounds related to the natural product fascaplysin, as novel inhibitors of CDK4/cyclin D1. We show all these molecules, prepared using the Suzuki-Miyaura reaction, being
Carine Aubry et al.
Organic & biomolecular chemistry, 4(5), 787-801 (2006-02-24)
We present the design, synthesis, and biological activity of three classes of tryptamine derivatives, which are non-planar analogues of the toxic anti-cancer agent fascaplysin. We show these compounds to be selective inhibitors of CDK4 over CDK2, the most active compound
Diane M Kanter et al.
Nucleic acids research, 39(7), 2580-2592 (2010-11-27)
Sld2 is essential for the initiation of DNA replication, but the mechanism underlying its role in replication is not fully understood. The S-phase cyclin dependent kinase (S-CDK) triggers the association of Sld2 with Dpb11, and a phosphomimetic mutation of Sld2
F Toribio et al.
Journal of chromatography. B, Biomedical applications, 684(1-2), 77-97 (1996-09-20)
The different preparative techniques and related analytical methods used for purification of glutathione peroxidase, glutathione transferase and glutathione reductase, described in papers published in the last ten years, have been reviewed in this article. Among the different purification techniques, chromatography
Pablo C Echeverría et al.
Molecular and cellular biology, 29(17), 4788-4797 (2009-07-08)
Glucocorticoid receptor (GR) is cytoplasmic in the absence of ligand and localizes to the nucleus after steroid binding. Previous evidence demonstrated that the hsp90-based heterocomplex bound to GR is required for the efficient retrotransport of the receptor to the nuclear

Contenu apparenté

Tests, réactifs et protocoles permettant d'étudier les interactions protéines/protéines in vitro par différentes méthodes : pull-down ou GST pull-down, purification par affinité en tandem (TAP pour "Tandem Affinity Purification") et co-immunoprécipitation.

Investigate in vitro protein-protein interactions with pull-down assays, utilizing affinity, GST pull-down, TAP, and co-immunoprecipitation methods.

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