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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1979 1
1986 3
1987 1
1988 2
1989 3
1990 3
1992 2
1993 2
1995 1
1997 1
1998 1
1999 1
2001 1
2003 1
2024 0

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23 results

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Page 1
Characterization of S-hexylglutathione-binding proteins of human hepatocellular carcinoma: separation of enoyl-CoA isomerase from an Alpha class glutathione transferase form.
Kajihara-Kano H, Hayakari M, Satoh K, Tomioka Y, Mizugaki M, Tsuchida S. Kajihara-Kano H, et al. Biochem J. 1997 Dec 1;328 ( Pt 2)(Pt 2):473-8. doi: 10.1042/bj3280473. Biochem J. 1997. PMID: 9371703 Free PMC article.
Recent studies have revealed binding of mitochondrial enoyl-CoA isomerase (ECI) to S-hexylglutathione-Sepharose, an affinity matrix used for purification of glutathione transferases (GSTs), and the enzyme has been suggested to be identical with the Alpha clas …
Recent studies have revealed binding of mitochondrial enoyl-CoA isomerase (ECI) to S-hexylglutathione-Sepharose, an aff …
Purification and physical characterization of glutathione S-transferase K. Differential use of S-hexylglutathione and glutathione affinity matrices to isolate a novel glutathione S-transferase from rat liver.
Hayes JD. Hayes JD. Biochem J. 1986 Feb 1;233(3):789-98. doi: 10.1042/bj2330789. Biochem J. 1986. PMID: 3707526 Free PMC article.
A novel hepatic enzyme, glutathione S-transferase K, is described that, unlike previously characterized transferases, possesses little affinity for S-hexylglutathione-Sepharose 6B but can be isolated because it binds to a glutathione affinity matrix. A purifi …
A novel hepatic enzyme, glutathione S-transferase K, is described that, unlike previously characterized transferases, possesses little affin …
Selective elution of rodent glutathione S-transferases and glyoxalase I from the S-hexyglutathione-Sepharose affinity matrix.
Hayes JD. Hayes JD. Biochem J. 1988 Nov 1;255(3):913-22. doi: 10.1042/bj2550913. Biochem J. 1988. PMID: 3214431 Free PMC article.
A further fraction (pool 5) can be prepared from material that does not bind S-hexylglutathione-Sepharose and is obtained by chromatography on glutathione-Sepharose. 4. ...GST YkYk and YoYo, which have weak affinities for S-hexylglutathione-S …
A further fraction (pool 5) can be prepared from material that does not bind S-hexylglutathione-Sepharose and is obtain …
Glutathione disulfide-stimulated Mg2+-ATPase of human erythrocyte membranes.
Kondo T, Kawakami Y, Taniguchi N, Beutler E. Kondo T, et al. Proc Natl Acad Sci U S A. 1987 Nov;84(21):7373-7. doi: 10.1073/pnas.84.21.7373. Proc Natl Acad Sci U S A. 1987. PMID: 2959960 Free PMC article.
Erythrocyte membranes that were depleted of extrinsic proteins were solubilized in 0.5% Triton X-100. Affinity chromatography on S-hexylglutathione-Sepharose 6B, with elution by a linear gradient of S-hexyl-glutathione, resulted in the resolution of two peaks …
Erythrocyte membranes that were depleted of extrinsic proteins were solubilized in 0.5% Triton X-100. Affinity chromatography on S- …
Purification and partial characterization of glyoxalase I from bovine brain.
Lupidi G, Venardi G, Bollettini M, Marmocchi F, Rotilio G. Lupidi G, et al. Prep Biochem Biotechnol. 2001 Aug;31(3):305-16. doi: 10.1081/PB-100104911. Prep Biochem Biotechnol. 2001. PMID: 11513094
Glyoxalase I was purified to homogeneity from bovine brain using affinity chromatography on S-hexylglutathione-Sepharose 6B with a yield of 22%. The enzyme was a dimer (44,000 Daltons) composed of, apparently, identical subunits (22,000 Daltons), as shown by …
Glyoxalase I was purified to homogeneity from bovine brain using affinity chromatography on S-hexylglutathione-Sepharose …
Comparison of glyoxalase I purified from yeast (Saccharomyces cerevisiae) with the enzyme from mammalian sources.
Marmstål E, Aronsson AC, Mannervik B. Marmstål E, et al. Biochem J. 1979 Oct 1;183(1):23-30. doi: 10.1042/bj1830023. Biochem J. 1979. PMID: 393249 Free PMC article.
Glyoxalase I from yeast (Saccharomyces cerevisiae) purified by affinity chromatography on S-hexylglutathione-Sepharose 6B was characterized and compared with the enzyme from rat liver, pig erythrocytes and human erythrocytes. ...
Glyoxalase I from yeast (Saccharomyces cerevisiae) purified by affinity chromatography on S-hexylglutathione-Sepharose …
Expression of glyoxalase, glutathione peroxidase and glutathione S-transferase isoenzymes in different bovine tissues.
Hayes JD, Milner SW, Walker SW. Hayes JD, et al. Biochim Biophys Acta. 1989 Jan 19;994(1):21-9. doi: 10.1016/0167-4838(89)90057-5. Biochim Biophys Acta. 1989. PMID: 2909253
The pi class Yf subunit (24.8 kDa) was detected in large amounts in the adrenals, brain, heart, lung and spleen, but not in kidney or liver. (5) Gradient affinity elution of S-hexylglutathione-Sepharose showed that the bovine proteins that bind to this matrix …
The pi class Yf subunit (24.8 kDa) was detected in large amounts in the adrenals, brain, heart, lung and spleen, but not in kidney or liver. …
Expression of an abundant alpha-class glutathione S-transferase in bovine and human adrenal cortex tissues.
Meikle I, Hayes JD, Walker SW. Meikle I, et al. J Endocrinol. 1992 Jan;132(1):83-92. doi: 10.1677/joe.0.1320083. J Endocrinol. 1992. PMID: 1737963
We describe the purification and characterization of an abundant alpha-class GST from this tissue that has not been identified previously because of its failure to bind to S-hexylglutathione-Sepharose 6B (S-hexG-Ag). This enzyme has been affinity purified on …
We describe the purification and characterization of an abundant alpha-class GST from this tissue that has not been identified previously be …
S-(4-azidophenacyl)[35S]glutathione photoaffinity labeling of rat liver plasma membrane-associated proteins.
Kunst M, Sies H, Akerboom TP. Kunst M, et al. Biochim Biophys Acta. 1989 Jun 26;982(1):15-23. doi: 10.1016/0005-2736(89)90168-5. Biochim Biophys Acta. 1989. PMID: 2742884
Isoelectric focusing of the CMV indicated the presence of basic soluble GST subunits. S-Hexylglutathione-Sepharose affinity chromatography showed reversible binding of photolabeled proteins at 25-29 kDa. ...
Isoelectric focusing of the CMV indicated the presence of basic soluble GST subunits. S-Hexylglutathione-Sepharose affi …
23 results