• Western blot analysis of lysate from HepG2 cells, using GGT1 Antibody.
  • Immunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:100
  • Immunohistochemical analysis of paraffin-embedded human-kidney, antibody was diluted at 1:100
  • Western blot analysis of HepG2 cells using GGT1 Polyclonal Antibody.. Secondary antibody was diluted at 1:20000

Anti-GGT1 antibody (21-70 aa) (STJ96631)

SKU:
STJ96631

Current Stock:
Host: Rabbit
Applications: WB/IHC/IF/ELISA
Reactivity: Human/Rat/Mouse
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description: Rabbit polyclonal antibody anti-Glutathione hydrolase 1 proenzyme (21-70 aa) is suitable for use in Western Blot, Immunohistochemistry, Immunofluorescence and ELISA research applications.
Clonality: Polyclonal
Conjugation: Unconjugated
Isotype: IgG
Formulation: Liquid in PBS containing 50% Glycerol, 0.5% BSA and 0.02% Sodium Azide.
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/mL
Dilution Range: WB 1:500-1:2000
IHC-P 1:100-300
ELISA 1:20000
IF 1:50-200
Storage Instruction: Store at-20°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.
Gene Symbol: GGT1
Gene ID: 2678
Uniprot ID: GGT1_HUMAN
Immunogen Region: 21-70 aa
Specificity: GGT1 Polyclonal Antibody detects endogenous levels of GGT1 protein.
Immunogen: The antiserum was produced against synthesized peptide derived from the N-terminal region of human GGT1 at the amino acid range 21-70
Post Translational Modifications N-glycosylated on both chains. Contains hexoses, hexosamines and sialic acid residues. Glycosylation profiles tested in kidney and liver tissues reveal the presence of tissue-specific and site-specific glycan composition, despite the overlap in composition among the N-glycans. A total of 36 glycan compositions, with 40 unique structures are observed. Up to 15 different glycans are observed at a single site, with site-specific variation in glycan composition. The difference in glycosylation profiles in the 2 tissues do not affect the enzyme activity. Cleaved by autocatalysis into a large and a small subunit and the autocatalytic cleavage is essential to the functional activation of the enzyme.
Function Cleaves the gamma-glutamyl bond of extracellular glutathione (gamma-Glu-Cys-Gly), glutathione conjugates (such as maresin conjugate (13R)-S-glutathionyl-(14S)-hydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoate, MCTR1) and other gamma-glutamyl compounds (such as leukotriene C4, LTC4). The metabolism of glutathione by GGT1 releases free glutamate and the dipeptide cysteinyl-glycine, which is hydrolyzed to cysteine and glycine by dipeptidases. In the presence of high concentrations of dipeptides and some amino acids, can also catalyze a transpeptidation reaction, transferring the gamma-glutamyl moiety to an acceptor amino acid to form a new gamma-glutamyl compound. Contributes to cysteine homeostasis, glutathione homeostasis and in the conversion of the leukotriene LTC4 to LTD4. Isoform 3: Seems to be inactive.
Protein Name Glutathione Hydrolase 1 Proenzyme
Gamma-Glutamyltransferase 1
Gamma-Glutamyltranspeptidase 1
Ggt 1
Leukotriene-C4 Hydrolase
Cd Antigen Cd224 Cleaved Into - Glutathione Hydrolase 1 Heavy Chain - Glutathione Hydrolase 1 Light Chain
Database Links Reactome: R-HSA-174403
Reactome: R-HSA-2142691
Reactome: R-HSA-5423646
Reactome: R-HSA-5579022
Reactome: R-HSA-9035968
Reactome: R-HSA-9664535
Reactome: R-HSA-9753281
Cellular Localisation Cell Membrane
Single-Pass Type Ii Membrane Protein
Alternative Antibody Names Anti-Glutathione Hydrolase 1 Proenzyme antibody
Anti-Gamma-Glutamyltransferase 1 antibody
Anti-Gamma-Glutamyltranspeptidase 1 antibody
Anti-Ggt 1 antibody
Anti-Leukotriene-C4 Hydrolase antibody
Anti-Cd Antigen Cd224 Cleaved Into - Glutathione Hydrolase 1 Heavy Chain - Glutathione Hydrolase 1 Light Chain antibody
Anti-GGT1 antibody
Anti-GGT antibody

Information sourced from Uniprot.org

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