COMT (D4N6M) Rabbit mAb (BSA and Azide Free) #84315
- WB
- IHC
Supporting Data
REACTIVITY | H |
SENSITIVITY | Endogenous |
MW (kDa) | 24, 28 |
Source/Isotype | Rabbit IgG |
Application Key:
- WB-Western Blotting
- IHC-Immunohistochemistry
Species Cross-Reactivity Key:
- H-Human
Product Information
Product Usage Information
This formulation is ideal for use with technologies requiring specialized or custom antibody labeling, including fluorophores, metals, lanthanides, and oligonucleotides. It is not recommended for ChIP, ChIP-seq, CUT&RUN or CUT&Tag assays. If you require a carrier free formulation for chromatin profiling, please contact us. Optimal dilutions/concentrations should be determined by the end user.
BSA and Azide Free antibodies are quality control tested by size exclusion chromatography (SEC) to determine antibody integrity.
Formulation
For standard formulation of this product see product #14368
Storage
Specificity / Sensitivity
Species Reactivity:
Source / Purification
Background
In addition to inactivating endogenous catecholamines, COMT can also inhibit catechol-based drugs used to treat a number of disorders, including Parkinson's disease and schizophrenia. Research studies using COMT inhibitors indicate that these reagents can prolong the bioavailability of psychoactive drugs such as levodopa by preventing O-methylation and subsequent degradation (6). A Val158Met polymorphism in the corresponding COMT gene reduces COMT enzymatic activity and leads to increased cortical dopamine levels (7). Several research studies suggest that this reduced COMT activity is associated with a large number of mental disorders, including schizophrenia, bipolar disorder, attention deficit hyperactivity disorder, obsessive-compulsive disorder, and anorexia nervosa (reviewed in 8).
- Weinshilboum, R.M. et al. (1999) Annu Rev Pharmacol Toxicol 39, 19-52.
- Roth, J.A. (1992) Rev Physiol Biochem Pharmacol 120, 1-29.
- Tenhunen, J. and Ulmanen, I. (1993) Biochem J 296 ( Pt 3), 595-600.
- Männistö, P.T. et al. (1992) Prog Drug Res 39, 291-350.
- Männistö, P.T. and Kaakkola, S. (1999) Pharmacol Rev 51, 593-628.
- Rivest, J. et al. (1999) Can J Neurol Sci 26 Suppl 2, S34-8.
- Chen, J. et al. (2004) Am J Hum Genet 75, 807-21.
- Hosák, L. (2007) Eur Psychiatry 22, 276-81.
Limited Uses
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