GSTZ1 Antibody

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Description

Introduction to GSTZ1 Antibody

The GSTZ1 antibody is a research tool designed to detect and quantify glutathione S-transferase zeta 1 (GSTZ1), a critical enzyme encoded by the GSTZ1 gene located on chromosome 14q24.3 . GSTZ1, also known as maleylacetoacetate isomerase (MAAI), plays dual roles in detoxification (via glutathione conjugation) and intermediary metabolism (tyrosine/phenylalanine catabolism) . Deficiencies in GSTZ1 are linked to metabolic disorders (e.g., alkaptonuria) and cancer progression . Antibodies targeting GSTZ1 enable researchers to study its expression, localization, and functional roles in disease models.

Research Applications and Findings

GSTZ1 antibodies have been instrumental in uncovering the enzyme’s role in disease mechanisms:

Hepatocellular Carcinoma (HCC)

  • Tumor Suppressor Role: GSTZ1 deficiency promotes HCC proliferation by activating the NRF2/IGF1R axis, leading to oxidative stress and metabolic dysregulation . Studies using GSTZ1-knockout (KO) models showed increased hepatocarcinogenesis in mice .

  • Sorafenib Resistance: Overexpression of GSTZ1 sensitizes HCC cells to sorafenib by enhancing ferroptosis, while KO cells exhibit resistance .

Metabolic Disorders

  • GSTZ1 is critical for detoxifying dichloroacetic acid (DCA), preventing hepatotoxicity . Genetic variations (e.g., E32K haplotype) reduce GSTZ1 activity, influencing drug metabolism .

Oxidative Stress Regulation

  • Engineered GSTZ1 variants mimic glutathione peroxidase (GPX), offering therapeutic potential against neurodegenerative diseases and atherosclerosis .

Key Research Insights

Study FocusMechanism/OutcomeCitation
GSTZ1 in HCCGSTZ1 deficiency upregulates IGF1R, promoting tumor growth via antiapoptotic pathways
Sorafenib ResistanceGSTZ1 loss activates NRF2/GPX4 axis, reducing ferroptosis and drug efficacy
Genetic PolymorphismsE32K haplotype reduces GSTZ1 activity, slowing DCA metabolism
Antioxidant EngineeringSeleno-hGSTZ1–1 exhibits GPX-like activity, mitigating oxidative damage

Clinical and Therapeutic Implications

  • Diagnostic Potential: GSTZ1 expression correlates with HCC prognosis; low levels predict poor survival .

  • Therapeutic Targets: Inhibiting NRF2 or IGF1R may counteract GSTZ1 deficiency in HCC . Combining sorafenib with ferroptosis inducers (e.g., RSL3) could overcome drug resistance .

Challenges and Future Directions

  • Species Cross-Reactivity: Most antibodies are validated for human, mouse, and rat tissues, but cross-reactivity in other models requires further study .

  • Functional Variants: Haplotype-specific effects (e.g., KGT, KGM) on GSTZ1 activity necessitate personalized approaches in metabolic therapies .

Product Specs

Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
Made-to-order (14-16 weeks)
Synonyms
GSTZ1 antibody; GST18 antibody; GSTZ antibody; At2g02390 antibody; T16F16.18 antibody; Glutathione S-transferase Z1 antibody; AtGSTZ1 antibody; EC 2.5.1.18 antibody; GST class-zeta member 1 antibody; Glutathione S-transferase 18 antibody; Maleylacetone isomerase antibody; MAI antibody; EC 5.2.1.- antibody
Target Names
GSTZ1
Uniprot No.

Target Background

Function
GSTZ1 functions as a maleylacetone isomerase. It also catalyzes the glutathione-dependent dehalogenation of dichloroacetic acid to glyoxylic acid. In vitro studies have demonstrated that GSTZ1 possesses glutathione peroxidase activity towards cumene hydroperoxide and linoleic acid-13-hydroperoxide.
Gene References Into Functions
  1. The specific shape of the active site in AtGSTZ-1 is essential to its activity. PMID: 20622445
  2. Mutants W15R, C19Y, R22H/K83E, P61S, S73P, S109P, and Q112R have been shown to exhibit activity levels lower than 1% of the wild-type. PMID: 20331431
Database Links

KEGG: ath:AT2G02390

STRING: 3702.AT2G02390.3

UniGene: At.10192

Protein Families
GST superfamily, Zeta family
Subcellular Location
Cytoplasm, cytosol.

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