| Catalog No. | Size | Price (USD) |
| 14237-RP01-100 | 100 µL | $147.96 |
| 14237-RP01-200 | 200 µL | $251.64 |
| 14237-RP01-400 | 400 µL | $355.32 |
General Information
| Product name | Anti-GSTZ1 Antibody, Rabbit Polyclonal |
| Validated applications | ELISA (FAQ Protocol) |
| Species reactivity | Reacts with: Human |
| Specificity | Human GSTZ1 |
| Immunogen | Recombinant Human GSTZ1 protein (Catalog#14237-H07E) |
| Preparation | Produced in rabbits immunized with purified, recombinant Human GSTZ1 (rh GSTZ1; Catalog#14237-H07E; NP_665877.1; Met1-Ala216). Total IgG was purified by Protein A affinity chromatography. |
| Source | Polyclonal Rabbit IgG |
| Purification | Protein A |
| Formulation | 0.2 μm filtered solution in PBS |
| Conjugate | Unconjugated |
| Form | Liquid |
| Shipping | This antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. |
| Storage | 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. Avoid repeated freeze-thaw cycles. |
Synonyms: Anti-GSTZ1-1 Antibody; Anti-MAAI Antibody; Anti-MAAID Antibody; Anti-MAI Antibody
Background Information
| Full Name | glutathione S-transferase zeta 1 |
| Description | GSTZ1 (Glutathione S-Transferase Zeta 1) is a Protein Coding gene. 3 alternatively spliced human isoforms have been reported. GSTZ1 gene is a member of the glutathione S-transferase (GSTs) super-family which encodes multifunctional enzymes important in the detoxification of electrophilic molecules, including carcinogens, mutagens, and several therapeutic drugs, by conjugation with glutathione. GSTZ1 is a bifunctional protein that has minimal glutathione-conjugating activity with ethacrynic acid and 7-chloro-4-nitrobenzo-2-oxa-1,3-diazole and maleylacetoacetate isomerase activity. GSTZ1 catalyzes the glutathione-dependent oxygenation of dichloroacetic acid to glyoxylic acid. GSTZ1 participates in the catabolism of phenylalanine and tyrosine. Thus defects in GSTZ1 cause harsh metabolic disorders including alkaptonuria, phenylketonuria, and tyrosinemia. |
| References |
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