Mouse Monoclonal CYP3A5 antibody. Suitable for WB, IHC-P and reacts with Synthetic peptide - Human, Human samples. Cited in 1 publication. Immunogen corresponding to Synthetic Peptide within Human CYP3A5.
IgG1
Mouse
Preservative: 0.08% Sodium azide
Constituents: PBS
Liquid
Monoclonal
WB | IHC-P | |
---|---|---|
Human | Expected | Tested |
Synthetic peptide - Human | Tested | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide - Human | Dilution info 1.00000-2.00000 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1.00000-5.00000 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Synthetic peptide - Human | Dilution info - | Notes - |
Select an associated product type
A cytochrome P450 monooxygenase involved in the metabolism of steroid hormones and vitamins (PubMed:2732228, PubMed:10681376, PubMed:11093772, PubMed:12865317). 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 (PubMed:12865317, PubMed:2732228, PubMed:10681376, PubMed:11093772). Exhibits high catalytic activity for the formation of catechol estrogens from 17beta-estradiol (E2) and estrone (E1), namely 2-hydroxy E1 and E2 (PubMed:12865317). Catalyzes 6beta-hydroxylation of the steroid hormones testosterone, progesterone, and androstenedione (PubMed:2732228). Catalyzes the oxidative conversion of all-trans-retinol to all-trans-retinal, a rate-limiting step for the biosynthesis of all-trans-retinoic acid (atRA) (PubMed:10681376). Further metabolizes all trans-retinoic acid (atRA) to 4-hydroxyretinoate and may play a role in hepatic atRA clearance (PubMed:11093772). Also involved in the oxidative metabolism of xenobiotics, including calcium channel blocking drug nifedipine and immunosuppressive drug cyclosporine (PubMed:2732228).
Cytochrome P450 3A5, CYPIIIA5, Cytochrome P450-PCN3, CYP3A5
Mouse Monoclonal CYP3A5 antibody. Suitable for WB, IHC-P and reacts with Synthetic peptide - Human, Human samples. Cited in 1 publication. Immunogen corresponding to Synthetic Peptide within Human CYP3A5.
Cytochrome P450 3A5, CYPIIIA5, Cytochrome P450-PCN3, CYP3A5
IgG1
Mouse
Preservative: 0.08% Sodium azide
Constituents: PBS
Liquid
Monoclonal
F18 P3 B6
Blue Ice
-20°C
Upon delivery aliquot
Avoid freeze / thaw cycle
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This supplementary information is collated from multiple sources and compiled automatically.
CYP3A5 also known as cytochrome P450 3A5 is an enzyme involved in drug metabolism. It is part of the cytochrome P450 superfamily. The enzyme has a molecular weight of approximately 57 kDa. Scientists have identified CYP3A5 as an important player in the oxidative metabolism of various xenobiotics and endogenous compounds. It is predominantly expressed in the liver but is also found in the kidney and intestines. Variability in CYP3A5 expression across individuals can significantly impact drug clearance rates and pharmacokinetics.
CYP3A5 plays a significant role in the metabolism of many drugs and steroid hormones. This ability stems from its function as a monooxygenase in the metabolism of both exogenous and endogenous substrates. CYP3A5 is not necessarily part of a larger enzyme complex but it often acts in concert with other CYP3A enzymes within the liver. Variability in gene expression can result in different metabolizing capacities among individuals which scientists often relate to genetic polymorphisms that affect the CYP3A5*3 allele.
CYP3A5 is integral to the steroid hormone biosynthesis and drug metabolism pathways. It interacts closely with CYP3A4 frequently working together to metabolize substrates such as cortisol and testosterone. The pathway involving drug metabolism highlights the importance of these enzymes in the detoxification and clearance of pharmaceuticals which may influence drug efficacy and safety in patients. Through its involvement in steroid hormone biosynthesis CYP3A5 coordinates with other enzymes to regulate the levels of active hormones contributing to hormonal balance.
Scientists have linked variations in CYP3A5 expression and activity to hypertension and cancer. The role of CYP3A5 in hypertension is of particular interest due to its involvement in the metabolism of cortisol a hormone influencing blood pressure. Additionally altered CYP3A5 activity can affect the activation and clearance of chemotherapeutic agents impacting treatment outcomes in cancer. Researchers have noted that CYP3A5 shares functional relationships with proteins such as P-glycoprotein which plays roles in drug transport and resistance further connecting it to treatment efficacy and safety in these diseases.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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All lanes: Western blot - Anti-CYP3A5 antibody [F18 P3 B6] (ab56076) at 2 µg/mL
Lane 1: CYP3A4 recombinant CYP450 protein
Lane 2: CYP3A5 recombinant CYP450 protein
Lane 3: CYP3A7 recombinant CYP450 protein
Predicted band size: 57 kDa
Observed band size: 57 kDa
Lane 1: Molecular weight markers
Lanes 10, 2, 3, 4, 5, 6, 7, 8 and 9: Western blot - Anti-CYP3A5 antibody [F18 P3 B6] (ab56076) at 2 µg/mL
Lane 2: CYP1A1 recombinant protein
Lane 3: CYP2C18 recombinant protein
Lane 4: CYP2C19 recombinant protein
Lane 5: CYP2D6 recombinant protein
Lane 6: CYP4F2 recombinant protein
Lane 7: CYP4F3 recombinant protein
Lane 8: CYP3A5 recombinant protein
Lane 9: CYP3A7 recombinant protein
Lane 10: Negative control
Predicted band size: 57 kDa
Observed band size: 57 kDa
Oesophageal squamous cell carcinoma tissue stained with ab56076 at 5 µg/ml.
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