Glutathione

Glycine is a non-chiral amino acid that can be synthesized in the body from the amino acid serine by Serine Hydroxymethyltransferase. Acts as an inhibitory neurotransmitter Shown to block NMDA-stimulated dopamine release in fetal mesencephalic cell

Isopropyl b-D-1-thiogalactopyranoside is a non-metabolizable galactose analog that induces expression of the lac operon in Escherichia coli. It functions by binding to the lac repressor and altering its conformation.

Glutathione suppresses human immunodeficiency virus expression in chronically infected monocytic cells. It is a useful tripeptide involved in many aspects of metabolism, including transport of g-glutanyl amino acids and reductive cleavage of

CAS No.: 10373-78-1

CAS No.: 10373-78-1

L-Cysteine is a proteinogenic amino acid incorporated into proteins as directed by the genetic code. The thiol-side chain participates in a variety of oxidation/reduction reactions within the cell.

Glutathione disulfide (GSSG) is the oxidised dimeric form of glutathione (GSH), which is a naturally occuring tripeptide that takes part in the bodies detoxification mechanisms and protects against oxidative damage. Glutathione Oxidized acts as

Glycine for use in electrophresis buffers.

Glycine is a non-chiral amino acid that can be synthesized in the body from the amino acid serine by Serine Hydroxymethyltransferase. Acts as an inhibitory neurotransmitter Shown to block NMDA-stimulated dopamine release in fetal mesencephalic cell

N-Acetyl-L-cysteine is an acetylated amino acid with antioxidant and mucolytic properties for isolation of mycobacteria from sputum. As a mucolytic agent, N-Acetyl-L-cysteine serves to dissipate disulfide bonds across mucoproteins, loosening and

N-Acetyl-L-cysteine is an acetylated amino acid with antioxidant and mucolytic properties. Dissipates disulfide bonds across mucoproteins Loosening and clearning the viscosity of sputum Increases cellular pools of free radical scavengers

Putrescine is a biogenic polyamine and precursor of spermidine. It is formed via decarboxylation of ornithine or by decarboxylation of arginine followed by hydrolysis.