Rabbit Polyclonal CYP2C8 antibody. Carrier free. Suitable for WB and reacts with Human samples. Immunogen corresponding to Recombinant Full Length Protein corresponding to Human Cytochrome P450 2C8.
pH: 7.4
Constituents: 100% PBS
WB | |
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Human | Tested |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/500.00000 - 1/1000.00000 | Notes - |
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A cytochrome P450 monooxygenase involved in the metabolism of various endogenous substrates, including fatty acids, steroid hormones and vitamins (PubMed:11093772, PubMed:14559847, PubMed:15766564, PubMed:19965576, PubMed:7574697). 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:11093772, PubMed:14559847, PubMed:15766564, PubMed:19965576, PubMed:7574697). Primarily catalyzes the epoxidation of double bonds of polyunsaturated fatty acids (PUFA) with a preference for the last double bond (PubMed:15766564, PubMed:19965576, PubMed:7574697). Catalyzes the hydroxylation of carbon-hydrogen bonds. Metabolizes all trans-retinoic acid toward its 4-hydroxylated form (PubMed:11093772). Displays 16-alpha hydroxylase activity toward estrogen steroid hormones, 17beta-estradiol (E2) and estrone (E1) (PubMed:14559847). Plays a role in the oxidative metabolism of xenobiotics. It is the principal enzyme responsible for the metabolism of the anti-cancer drug paclitaxel (taxol) (PubMed:26427316).
Cytochrome P450 2C8, CYPIIC8, Cytochrome P450 IIC2, Cytochrome P450 MP-12, Cytochrome P450 MP-20, Cytochrome P450 form 1, S-mephenytoin 4-hydroxylase, CYP2C8
Rabbit Polyclonal CYP2C8 antibody. Carrier free. Suitable for WB and reacts with Human samples. Immunogen corresponding to Recombinant Full Length Protein corresponding to Human Cytochrome P450 2C8.
pH: 7.4
Constituents: 100% PBS
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CYP2C8 also known as Cytochrome P450 2C8 is a member of the cytochrome P450 superfamily of enzymes. It has a molecular mass of approximately 56 kDa. CYP2C8 localizes mainly in the liver but can be found in smaller amounts in other tissues such as the kidney and heart. This enzyme plays a role in oxidizing various substances impacting drug metabolism. The enzyme achieves this by catalyzing reactions involved in drug detoxification and steroid synthesis.
CYP2C8 facilitates the metabolism of xenobiotics and endogenous compounds contributing to homeostasis. It forms part of the cytochrome P450 hepatic microsomal enzyme complex which contains multiple enzymes responsible for oxidative metabolism. CYP2C8 metabolizes several clinically important drugs including paclitaxel and amodiaquine as well as endogenous arachidonic acid impacting vascular biology.
This enzyme acts within the drug metabolism and arachidonic acid metabolism pathways. Within these pathways it works closely with other cytochrome P450 enzymes such as CYP3A4. The drug metabolism pathway requires CYP2C8 for phase I of drug processing which modifies drugs into more water-soluble compounds. In arachidonic acid metabolism CYP2C8 is important to forming bioactive epoxyeicosatrienoic acids that function as signaling molecules in tissues.
Dysregulation of CYP2C8 activity relates to conditions such as drug-induced liver injury and cardiovascular diseases. Variants in the CYP2C8 gene can lead to altered enzyme activity influencing drug response and toxicity. Furthermore its interaction with CYP2C9 in pharmacogenomic variability can affect patients' susceptibility to adverse drug reactions emphasizing the role in personalized medicine approaches.
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All lanes: Western blot - Anti-CYP2C8 antibody (ab103547) at 1/500 dilution
All lanes: Human liver tissue lysate at 50 µg
Predicted band size: 56 kDa
All lanes: Western blot - Anti-CYP2C8 antibody (ab103547) at 1/500 dilution
Lane 1: CYP2C8 transfected 293T cell lysate at 25 µg
Lane 2: Non-transfected 293T cell lysate at 25 µg
Predicted band size: 56 kDa
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