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H6783

Sigma-Aldrich

S-Hexylglutathione-Agarose

saline suspension

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About This Item

MDL number:
UNSPSC Code:
23151817
NACRES:
NA.56

form

saline suspension

extent of labeling

≥5 μmol per mL

matrix

Cross-linked 4% beaded agarose

matrix activation

epoxy

matrix attachment

amino

matrix spacer

12 atoms

storage temp.

2-8°C

Application

S-Hexylglutathione-agarose is an agarose conjugate in saline suspension used in affinity chromatography, protein chromatography, purification and detection, and recombinant protein expression and analysis. S-Hexylglutathione agarose has been used to inform vaccine development for major global diseases in livestock that infect humans, including the parasite Fasciola hepatica.

Physical form

Suspension in 0.5 M NaCl containing preservative

Disclaimer

For U.S. Customers: Contains mercury; Do not place in trash - dispose according to local, state, or federal laws.

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Marcel Deponte et al.
The Journal of biological chemistry, 282(39), 28419-28430 (2007-08-01)
Glyoxalase I (GloI) catalyzes the glutathione-dependent conversion of 2-oxoaldehydes to S-2-hydroxyacylglutathione derivatives. Studies on GloI from diverse organisms such as man, bacteria, yeast, and different parasites show striking differences among these potentially isofunctional enzymes as far as metal content and
M Moutiez et al.
The Biochemical journal, 310 ( Pt 2), 433-437 (1995-09-01)
Although trypanothione [T(S)2] is the major thiol component in trypanosomatidae, significant amounts of glutathione are present in Trypanosoma cruzi. This could be explained by the existence of enzymes using glutathione or both glutathione and T(S)2 as cofactors. To assess these
T Primiano et al.
Cancer research, 55(19), 4319-4324 (1995-10-01)
Oltipraz [5-(2-pyrazinyl)-4-methyl-1,2-dithiole-3-thione] protects against chemical carcinogenesis in several animal models and is currently under evaluation as a possible chemopreventive agent in humans. Ideally, clinical chemopreventive interventions use dosing regimens that maximize efficacy while minimizing toxicity. Toward this end, the chemopreventive
T Beeor-Tzahar et al.
FEBS letters, 366(2-3), 151-155 (1995-06-12)
A protein whose level is markedly increased upon exposure of cultured citrus cells and whole plants to NaCl, was shown to specifically catalyze the reduction of phosphatidylcholine hydroperoxide in the presence of glutathione. This enzymatic activity was shown to be
Rapid method for the determination of glutathione transferase isoenzymes in crude extracts.
Martinez-Lara, E., et al.
Journal of Chromatography A, 609(1-2), 141-146 (1992)

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