GSTZ1 Antibody (N-term) Blocking Peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Primary Accession | O43708 |
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Clone Names | 90415103 |
Gene ID | 2954 |
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Other Names | Maleylacetoacetate isomerase, MAAI, GSTZ1-1, Glutathione S-transferase zeta 1, GSTZ1, MAAI |
Target/Specificity | The synthetic peptide sequence used to generate the antibody AP9070a was selected from the N-term region of human GSTZ1. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay. |
Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
Name | GSTZ1 |
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Synonyms | MAAI |
Function | Bifunctional enzyme showing minimal glutathione-conjugating activity with ethacrynic acid and 7-chloro-4-nitrobenz-2-oxa-1,3- diazole and maleylacetoacetate isomerase activity. Has also low glutathione peroxidase activity with T-butyl and cumene hydroperoxides. Is able to catalyze the glutathione dependent oxygenation of dichloroacetic acid to glyoxylic acid. |
Cellular Location | Cytoplasm. |
Tissue Location | Mostly expressed in liver followed by kidney, skeletal muscle and brain. Also expressed in melanocytes, synovium, placenta, breast and fetal liver and heart |
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Provided below are standard protocols that you may find useful for product applications.
Background
GSTZ1 is a member of the glutathione S-transferase (GSTs) super-family which encodes multifunctional enzymes important in the detoxification of lectrophilic molecules, including carcinogens, mutagens, and several therapeutic drugs, by conjugation with glutathione. This enzyme also plays a significant role in the catabolism of phenylalanine and tyrosine. Thus defects in this enzyme may lead to severe metabolic disorders including alkaptonuria, phenylketonuria and tyrosinaemia.
References
Olshan,A.F., et.al., Mutat. Res. (2010) In pressJoslyn,G., et.al., Alcohol. Clin. Exp. Res. (2010) In press
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