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Endogenous antioxidant; reduces reactive oxygen species formed during cellular metabolism. Regulates activity of the redox sensitive transcription factor NF-κB. Cytoprotective.
|Storage||Store at +4°C|
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
|Solvent||Max Conc. mg/mL||Max Conc. mM|
Preparing Stock Solutions
The following data is based on the product molecular weight 307.32. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
|Concentration / Solvent Volume / Mass||1 mg||5 mg||10 mg|
|1 mM||3.25 mL||16.27 mL||32.54 mL|
|5 mM||0.65 mL||3.25 mL||6.51 mL|
|10 mM||0.33 mL||1.63 mL||3.25 mL|
|50 mM||0.07 mL||0.33 mL||0.65 mL|
References are publications that support the biological activity of the product.
Sen et al (1999) Glutathione homeostasis in response to exercise training and nutritional supplements. Mol.Cell.Biochem. 196 31 PMID: 10448900
Kerksick et al (2005) The antioxidant role of glutathione and N-acetyl-cysteine supplements and exercise-induced oxidative stress. J.Int.Soc.Sports Nutr. 2 38 PMID: 18500954
If you know of a relevant reference for L-Glutathione Reduced, please let us know.
Keywords: L-Glutathione Reduced, L-Glutathione Reduced supplier, Endogenous, antioxidant, NF-κB, cellular, metabolism, redox, cytoprotective, neuroprotective, GSH, Antioxidants, Amino, Acids, 5219, Tocris Bioscience
1 Citation for L-Glutathione Reduced
Citations are publications that use Tocris products. Selected citations for L-Glutathione Reduced include:
Das et al (2017) Loss of Merlin induces metabolomic adaptation that engages dependence on Hedgehog signaling. Sci Rep 7 40773 PMID: 28112165
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Reviews for L-Glutathione Reduced
Average Rating: 5 (Based on 3 Reviews.)
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used at 14mM aq. solution for kinetics experiments.
used it for generating a reducing environment in-vitro
GSH was used at a concentration 10µM and was well tolerated by the cells. BV2 cells were pre incubated with the inhibitor for one and then treated with 1µM LPA. Western blot analysis revealed that GSH incubation did not abolish the LPA induced expression of pAMPK in BV2 microglia cells.
MG-63 cells were incubated with GSH (10 μM) for 30 min prior to 15d-PGJ2 treatment (20 μM) for 24 h to follow apoptotic markers using Western blot. GSH inhibited 15d-PGJ2-induced PARP and Caspase-3 cleavage.
Literature in this Area
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