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{{/_source.additionalInfo}}Anti-Cytochrome P450 1A2 [3B8C1]
(Cat#: 152163)
Description
| Cat# | 152163 |
| Applications | IHC, WB |
| Antigen/Gene or Protein Targets | Cytochrome P450 1A2 (CYP1A2) |
| Reactivity | Human |
| Relevance | Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It oxidizes a variety of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics. Most active in catalyzing 2-hydroxylation. Caffeine is metabolized primarily by cytochrome CYP1A2 in the liver through an initial N3-demethylation. Also acts in the metabolism of aflatoxin B1 and acetaminophen. Participates in the bioactivation of carcinogenic aromatic and heterocyclic amines. Catalizes the N-hydroxylation of heterocyclic amines and the O-deethylation of phenacetin. |
| Host | Mouse |
| Immunogen | Rat cytochrome P450 proteins |
| Positive Control |
IHC: formalin-fixed, paraffin-embedded normal liver sections Western blot: recombinant P450 |
| Subclass | IgG1 kappa |
| Myeloma Used | P3X63Ag8.653 |
| Strain | Balb/c |
| Research Area | Cancer, Cardiovascular, Cell Signaling & Signal Transduction, Metabolism |
| References | Profiling the expression of cytochrome P450 in breast cancer. Europe PMC ID: 20716162 |
For Research Use Only.
