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Anti-P450 1A2 antibody

产品货号 产品 品牌 单位 存货 价格 促销价 数量  
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Anti-P450 1A2 antibody
洱畔/Erpan Tech 有货

产品特性        

Product type: Primary antibody
Antigen: P450 1A2
Immunogen: KLH conjugated synthetic peptide derived from human P450 1A2/CYP1A2 221-320/513
Species immunized: Rabbit
Isotype: IgG
Applications: Western Blot (1:1000-1:2500);Flow Cytometry(2ug/Test)
Reactivity: Human, Mouse, Rat
Clonality (clone number): Polyclonal
Form: Liquid
Buffer: 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Concentration: 1mg/ml
Purity: Protein A affinity purified
Storage: Aliquot and freeze at -20℃. Avoid multiple freeze/thaw cycles.
Alternative names: CYP1A2
Cytochrome P450 1A2
cytochrome P450, family 1, subfamily a, polypeptide 2
Cytochrome P450 family 1 polypeptide 2
Cytochrome P450 subfamily I aromatic compound inducible polypeptide 2
Cyp1a2
CYPD45
P-450d
RATCYPD45
CYP1A2
CP12
CP 12
P3-450
Aryl hydrocarbon hydroxylase
Dioxin inducable P3 45
Flavoprotein linked monooxygenase
Microsomal monooxygenase
P450 4
P450 form 4
P450 P3
P450(PA)
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靶标信息

A cytochrome P450 monooxygenase involved in the metabolism of various endogenous substrates, including fatty acids, steroid hormones and vitamins (PubMed:9435160, PubMed:10681376, PubMed:11555828, PubMed:12865317, PubMed:19965576). 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) (PubMed:9435160, PubMed:10681376, PubMed:11555828, PubMed:12865317, PubMed:19965576). Catalyzes the hydroxylation of carbon-hydrogen bonds (PubMed:11555828, PubMed:12865317). Exhibits high catalytic activity for the formation of hydroxyestrogens from estrone (E1) and 17beta-estradiol (E2), namely 2-hydroxy E1 and E2 (PubMed:11555828, PubMed:12865317). Metabolizes cholesterol toward 25-hydroxycholesterol, a physiological regulator of cellular cholesterol homeostasis (PubMed:21576599). May act as a major enzyme for all-trans retinoic acid biosynthesis in the liver. Catalyzes two successive oxidative transformation of all-trans retinol to all-trans retinal and then to the active form all-trans retinoic acid (PubMed:10681376). Primarily catalyzes stereoselective epoxidation of the last double bond of polyunsaturated fatty acids (PUFA), displaying a strong preference for the (R,S) stereoisomer (PubMed:19965576). Catalyzes bisallylic hydroxylation and omega-1 hydroxylation of PUFA (PubMed:9435160). May also participate in eicosanoids metabolism by converting hydroperoxide species into oxo metabolites (lipoxygenase-like reaction, NADPH-independent) (PubMed:21068195). Plays a role in the oxidative metabolism of xenobiotics. Catalyzes the N-hydroxylation of heterocyclic amines and the O-deethylation of phenacetin (PubMed:14725854). Metabolizes caffeine via N3-demethylation (Probable).

产品来源

洱畔科技实验室

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