

| 货号 | PTX19895 |
|---|---|
| 品牌 | ProteoGenix |
| 描述 |
Anti-CYP3A4 Polyclonal Antibody (PTX19895) is a rabbit polyclonal antibody detecting CYPIIIA3,Cytochrome P450 3A4,1,4-cineole 2-exo-monooxygenase,CYP3A4,Cytochrome P450 3A3,Cytochrome P450 NF-25,Cytochrome P450-PCN1,CYPIIIA4,1,8-cineole 2-exo-monooxygenase,Albendazole monooxygenase (sulfoxide-forming),Nifedipine oxidase,Quinine 3-monooxygenase,CYP3A3,Cholesterol 25-hydroxylase,Cytochrome P450 HLp,Albendazole sulfoxidase in ELISA, IHC, WB. Suitable for Human.
Highlights
|
| 种属反应性 | Human |
| 应用 | ELISA, IHC, WB |
| 宿主 | Rabbit |
| 同种型 | IgG |
| 克隆类型 | Polyclonal |
| 免疫原 | E. coli - derived recombinant Human CYP3A4 (Gly26-Ala503). |
| 靶标 | CYPIIIA3,Cytochrome P450 3A4,1,4-cineole 2-exo-monooxygenase,CYP3A4,Cytochrome P450 3A3,Cytochrome P450 NF-25,Cytochrome P450-PCN1,CYPIIIA4,1,8-cineole 2-exo-monooxygenase,Albendazole monooxygenase (sulfoxide-forming),Nifedipine oxidase,Quinine 3-monooxygenase,CYP3A3,Cholesterol 25-hydroxylase,Cytochrome P450 HLp,Albendazole sulfoxidase |
| 纯化方式 | Purified by antigen affinity column. |
| Accession号 | P08684 |
| 状态 | Liquid |
| 保存溶液 | 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300. Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA. |
| 稳定性和存储 | Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt. |
| 背景 | Cytochrome P450 3A4 (CYP3A4) is a ~57 kDa protein. A cytochrome P450 monooxygenase involved in the metabolism of sterols, steroid hormones, retinoids and fatty acids. Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (NADPH--hemoprotein reductase). Catalyzes the hydroxylation of carbon-hydrogen bonds. Exhibits high catalytic activity for the formation of hydroxyestrogens from estrone (E1) and 17beta-estradiol (E2), namely 2-hydroxy E1 and E2, as well as D-ring hydroxylated E1 and E2 at the C-16 position. Plays a role in the metabolism of androgens, particularly in oxidative deactivation of testosterone. 1. Chen, H. et al. (2000) Drug metabolism and disposition: the biological fate of chemicals 28, 315-22. PMID: 10681376 2. Marill, J. et al. (2000) Molecular pharmacology 58, 1341-8. PMID: 11093772 3. Badawi, AF. et al. (2001) Metabolism: clinical and experimental 50, 1001-3. PMID: 11555828 4. Lee, AJ. et al. (2003) Endocrinology 144, 3382-98. PMID: 12865317 5. Lee, AJ. et al. (2003) Cancer research 63, 6532-6. PMID: 14559847 6. Krauser, JA. et al. (2004) European journal of biochemistry 271, 3962-9. PMID: 15373842 7. Choi, MH. et al. (2005) Drug metabolism and disposition: the biological fate of chemicals 33, 714-8. PMID: 15764715 8. Lucas, D. et al. (2010) Journal of lipid research 51, 1125-33. PMID: 19965576 9. Pratt-Hyatt, M. et al. (2010) Drug metabolism and disposition: the biological fate of chemicals 38, 2075-82. PMID: 20702771 10. Peng, CC. et al. (2011) Clinical pharmacology and therapeutics 89, 888-95. PMID: 21490593 |
| Note | For research use only. |

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