biological source
rabbit
Quality Level
recombinant
expressed in HEK 293 cells
conjugate
unconjugated
antibody form
purified antibody
antibody product type
primary antibodies
clone
2F2, recombinant monoclonal
description
recombinant, expressed in HEK 293 cells
product line
ZooMAb® learn more
form
lyophilized
mol wt
calculated mol wt 57.34 kDa
observed mol wt ~54 kDa
purified by
using Protein A
species reactivity
human
packaging
antibody small pack of 25
enhanced validation
recombinant expression
Learn more about Antibody Enhanced Validation
technique(s)
affinity binding assay: suitable
immunohistochemistry: suitable
western blot: suitable
isotype
IgG
epitope sequence
N-terminal half
Protein ID accession no.
UniProt accession no.
shipped in
ambient
storage temp.
2-8°C
Gene Information
human ... CYP3A4(1576)
General description
Cytochrome P450 3A4 (UniProt: P08684; also known as EC:1.14.14.1, 1,4-cineole 2-exo-monooxygenase, 1,8-cineole 2-exo-monooxygenase (EC:1.14.14.56), Albendazole monooxygenase (sulfoxide-forming) (EC:1.14.14.73), Albendazole sulfoxidase, CYPIIIA3, CYPIIIA4, Cholesterol 25-hydroxylase, Cytochrome P450 3A3, Cytochrome P450 HLp, Cytochrome P450 NF-25, Cytochrome P450-PCN1, Nifedipine oxidase, Quinine 3-monooxygenase (EC:1.14.14.55)) is encoded by the CYP3A4 (also known as CYP3A3) gene (Gene ID: 1576) in human. CYP3A4, a member of the cytochrome P450 superfamily, is a heme-containing monooxygenase enzyme. It consists of a single polypeptide chain with an active site containing a heme prosthetic group that facilitates its enzymatic function. CYP3A4 plays a pivotal role in the metabolism of xenobiotics and endogenous compounds, including drugs, toxins, steroids, and lipids. It catalyzes oxidation reactions, such as hydroxylation and demethylation, which are critical for detoxification and excretion. As the most abundant P450 isoform in the liver and intestine, CYP3A4 is responsible for the metabolism of nearly half of all clinically used drugs, including anticoagulants, immunosuppressants, and chemotherapeutics. CYP3A4 is predominantly expressed in hepatocytes and enterocytes, with additional expression noted in the kidney, brain, and other tissues. Its subcellular localization is primarily within the endoplasmic reticulum, where it interacts with co-factors like NADPH-cytochrome P450 reductase to facilitate electron transfer during enzymatic reactions. The activity of CYP3A4 is highly variable among individuals due to genetic polymorphisms, environmental factors, and regulatory influences such as inflammatory mediators and hormones. This variability can significantly affect drug efficacy and toxicity, contributing to interindividual differences in pharmacokinetics. CYP3A4 is regulated by nuclear receptors including pregnane X receptor (PXR) and vitamin D receptor (VDR), which respond to endogenous and exogenous ligands. These interactions mediate transcriptional activation of CYP3A4 under conditions of high xenobiotic exposure. The enzyme also has clinically significant interactions with other proteins, such as multidrug resistance protein 1 (MDR1), which impacts drug transport and metabolism. Furthermore, CYP3A4 is implicated in drug-drug interactions, particularly when inhibitors or inducers of the enzyme alter the metabolism of co-administered drugs, potentially leading to adverse effects like toxicity or therapeutic failure. This ZooMAb® recombinant monoclonal antibody, generated by our proprietary technology, offers significantly enhanced specificity, affinity, reproducibility, and stability over conventional monoclonals.
Immunogen
Application
Evaluated by Western Blotting with human liver microsomal preparation.
Western Blotting Analysis: A 1:10,000 dilution of this antibody detected CYP3A4 in human liver microsomal preparation.
Tested Applications
Immunohistochemistry (Paraffin) Analysis: A 1:100 dilution from a representative lot detected CYP3A4 in human liver tissue sections.
Affinity Binding Assay: A representative lot of this antibody bound with CYP3A4 peptide with at least ten thousand-fold (10,000X) higher affinity than with non-specific control peptide.
Note: Actual optimal working dilutions must be determined by end user as specimens and experimental conditions may vary with the end user.
Biochem/physiol Actions
Physical form
Preparation Note
Legal Information
Disclaimer
Not finding the right product?
Try our Product Selector Tool.
Regulatory Information
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
