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Anti-CYP2C19 antibody

SKU Product Brand Unit Availability Price Quantity  
AB-06-1249
Anti-CYP2C19 antibody
Erpan Tech In stock

Specifications        

Product Cat#: AB-06-1249
Product type: Primary antibody
Antigen: CYP2C19
Immunogen: KLH conjugated synthetic peptide derived from human CYP2C19 201-300/490
Species immunized: Rabbit
Isotype: IgG
Applications: Western Blot (1:500-1:2000); Immunohistochemistry-Paraffin (1:400-1:800)
Reactivity: Human
Clonality (clone number): Polyclonal
Form: Liquid
Buffer: 10mM Tris-HCl buffer (pH7.4), 1% BSA, 50% glycerol, 0.03% Proclin300.
Concentration: 1 mg/ml
Purity: Protein A affinity purified
Storage: Aliquot and freeze at -20℃. Avoid multiple freeze/thaw cycles.
Alternative names: AI266900
CYP2C
CYP2C19
CYP2C37
CYP2C50
Cyp2c54
CYP450-2C
CPCJ
CYPIIC17
CYPIIC19
EG404195
LOC293989
MGC109053
P450-11A
P450C2C
P450IIC19
CP2CJ_HUMAN Cytochrome P450 2C19
R)-limonene 6-monooxygenase
(S)-limonene 6-monooxygenase
(S)-limonene 7-monooxygenase
CYPIIC17
CYPIIC19
Cytochrome P450-11A
Cytochrome P450-254C
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Target information

A cytochrome P450 monooxygenase involved in the metabolism of polyunsaturated fatty acids (PUFA) (PubMed:18577768, PubMed:19965576, PubMed:20972997). 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:18577768, PubMed:19965576, PubMed:20972997). Catalyzes the hydroxylation of carbon-hydrogen bonds. Hydroxylates PUFA specifically at the omega-1 position (PubMed:18577768). Catalyzes the epoxidation of double bonds of PUFA (PubMed:20972997, PubMed:19965576). Also metabolizes plant monoterpenes such as limonene. Oxygenates (R)- and (S)-limonene to produce carveol and perillyl alcohol (PubMed:11950794). Responsible for the metabolism of a number of therapeutic agents such as the anticonvulsant drug S-mephenytoin, omeprazole, proguanil, certain barbiturates, diazepam, propranolol, citalopram and imipramine. Hydroxylates fenbendazole at the 4′ position (PubMed:23959307).

Provider

Erpantech Laboratory

download

MSDS-AB-06-1249.pdf (182 downloads )