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Anti-CYP3A4 Polyclonal Antibody (HY264014)

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Vista general
Número de catálogoHY264014
Descripción
Anti-CYP3A4 Polyclonal Antibody (HY264014) is a rabbit polyclonal antibody detecting CYP3A4 in ELISA, IHC, WB. Suitable for Human, Callithrix jacchus, and Macaca fascicularis.
Highlights
  • ●Affinity Purified — Minimal background and high purity for reliable results.
  • ●Multi-Application — Validated across multiple applications.
  • ●Multi-Species — Cross-reactive for translational research.
Reactividad de especiesHuman
AplicacionesELISA, IHC, WB
Especie huéspedRabbit
ClonalidadPolyclonal
IsotipoIgG
Inmunógeno E. coli - derived recombinant Human CYP3A4 (Gly26-Ala503).
Objetivo 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
Purificación Purified by antigen affinity column.
Número de acceso P08684
Forma Liquid
Buffer de almacenamiento 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.

Consulte la información específica del buffer en la copia impresa del datasheet o en el COA específico del lote.

Información de uso del producto
Aplicación Dilución
ELISA 1:5000-1:20000
IHC 1:50-1:500
WB 1:500-1:2000
Estabilidad y almacenamiento 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.
Fondo

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
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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
Nota For research use only.
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Formula
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Formula
C₁ × V₁ = C₂ × V₂
Enter any 3 of the 4 values to solve for the unknown.
Stock Solution
C₁ (Stock Conc.)
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V₁ (Stock Vol.)
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Working Solution
C₂ (Working Conc.)
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V₂ (Working Vol.)
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