Cell Signaling Technology

Product Pathways - Metabolism

CYP3A4 Antibody #12249

Applications Reactivity Sensitivity MW (kDa) Source
W IP H Mk Endogenous 50 Rabbit

Applications Key:  W=Western Blotting  IP=Immunoprecipitation
Reactivity Key:  H=Human  Mk=Monkey
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

Protocols

Specificity / Sensitivity

CYP3A4 Antibody recognizes endogenous levels of total CYP3A4 protein.

Source / Purification

Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human CYP3A4 protein. Antibodies are purified by protein A and peptide affinity chromatography.

Western Blotting

Western Blotting

Western blot analysis of extracts from various human tissues using CYP3A4 Antibody (upper) or β-Actin (D6A8) Rabbit mAb #8457 (lower).

Background

Cytochrome P450, subfamily 3A, polypeptide 4 (CYP3A4) is a mono-oxygenase enzyme (1) found in the endoplasmic reticulum membrane of liver and prostate microsomes. It is an important enzyme in drug metabolism; it catalyzes phase I oxidation reactions in approximately 50% of drugs in the modern market, as well as steroids, fatty acids, and some carcinogens (2). It is also involved in steroid and cholesterol synthesis (3,4). Expression of CYP3A4 can be induced by glucocorticoids, carcinogens, pesticides, and drugs, which can lead to drug interactions and toxicity (5).

  1. Gupta, R.P. et al. (2004) J Bone Miner Res 19, 680-8.
  2. Lynch, T. and Price, A. (2007) Am Fam Physician 76, 391-6.
  3. Pikuleva, I.A. (2006) Pharmacol Ther 112, 761-73.
  4. Tompkins, L.M. and Wallace, A.D. (2007) J Biochem Mol Toxicol 21, 176-81.
  5. Thummel, K.E. and Wilkinson, G.R. (1998) Annu Rev Pharmacol Toxicol 38, 389-430.

Application References

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Companion Products


For Research Use Only. Not For Use In Diagnostic Procedures.

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