In 1959 Shore, Burkhalter and Cohn (1) reported that the reaction of o-phthalaldehyde with histamine yielded a highly fluorescent reaction product which could be used for the assay of submicrogram amounts of histamine in biological tissues. Modification of this reaction and/or the extraction techniq
Enzymatic assay for glutathione
โ Scribed by Jacqueline E. Brehe; Helen B. Burch
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- English
- Weight
- 553 KB
- Volume
- 74
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
โฆ Synopsis
Methods for measuring total glutathione are described. These are based on the ability of glutathione and glutathione reductase (EC 1.6.4.2.) to catalyze the oxidation of NADPH by Ellman's reagent. Except for highest glutathione levels, NADP+ rather than the reduced Ellman compound is measured. For intermediate sensitivity (2 x lo-'* mol) NADP is measured stoichiometrically by conversion to NADPH and determination of fluorescence. For smaller amounts (lo-r4 mol) the NADP+ generated is amplified by enzymatic cycling. These procedures have been tested extensively on kidney and are probably applicable to tissues in general.
๐ SIMILAR VOLUMES
A method has been developed for the automated assay of glutathione and of related compounds utilizing an anion-exchange resin column in an amino acid analyzer. Reduced glutathione. glutathione disuhide, bis(y-glutamyl)cystine. y-glutamylcysteine, and cysteinylglycine have been assayed either directl
unc-25 in muscle cells (8) and GABAergic neurons (10), respectively. Without TSA, probe detection resulted in no hybridization signal. When TSA was performed, expression of unc-49 and unc-25 was detected in body wall muscles (Fig. ) and neurons, respectively. In conclusion, TSA is useful in the enh