Anti-GGT1 antibody

Anti-GGT1 antibody

• DataSheet
• Material Safety Data Sheets (MSDS)

Rabbit Polyclonal to Mouse GGT1

IHC-P

Mouse GGT1
Cross reactivity
React with
Human

GGT antibody; GTG antibody; CD224 antibody; GGT1 antibody; D22S672 antibody; D22S732 antibody; GGT antibody; dwg antibody; Ggtp antibody; CD224 antibody; GGT1 antibody; GGT-1 antibody; CD224 antibody; CD224 antibody; D22S672 antibody; D22S732 antibody; dwg antibody; gamma-glutamyl transpeptidase antibody; gamma-glutamyl transpeptidase antibody; gamma-glutamyltranspeptidase 1 antibody; gamma-glutamyltranspeptidase 1 antibody; GGT antibody; GGT antibody; GGT 1 antibody; GGT 1 antibody; Ggtp antibody; glutamyl transpeptidase antibody; glutathione hydrolase 1 antibody; glutathione hydrolase 1 antibody; GTG antibody; leukotriene-C4 hydrolase antibody; leukotriene-C4 hydrolase antibody

Rabbit IgG

Produced in rabbits immunized with a synthetic peptide corresponding to the center region of the Mouse GGT1, and purified by antigen affinity chromatography.

Polyclonal

0.2 μm filtered solution in PBS

This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free.
Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles.

GGT1 belongs to the gamma-glutamyltransferase protein family. Many members of this family have not yet been fully characterized and some of which may represent pseudogenes. GGT1 is composed of a heavy chain and a light chain. It catalyzes the transfer of the glutamyl moiety of glutathione to a variety of amino acids and dipeptide acceptors. GGT1 also initiates extracellular glutathione (GSH) breakdown, provides cells with a local cysteine supply and contributes to maintain intracelular GSH level. As part of the cell antioxidant defense mechanism, GGT1 can be detected in fetal and adult kidney and liver, adult pancreas, stomach, intestine, placenta and lung. Defects in GGT1 can cause glutathionuria which is known as an autosomal recessive disease.