PNMT Antibody (YA7151)
(Synonyms: PENT, PNMT, Phenylethanolamine N-methyltransferase, PNMTase, Noradrenaline N-methyltransferase)Based on 1 Customer Validation
PNMT Antibody (YA7151) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to PNMT.
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Host:
Rabbit
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Isotype:
IgG
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Application:
WB, ICC/IF
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Reactivity :
Human
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Formulation:
Supplied in 10mM phosphate buffered saline(pH 7.4) with 150mM sodium chloride, 0.05% BSA, 0.02% Proclin300 and 50% glycerol.
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Conjugation:
Non-conjugated
Applications
| Application |
WB
WB: Western Blot
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ICC/IF
ICC/IF: Immunocytochemistry/
Immunofluorescence |
|---|---|---|
| Dilution Ratio | 1:500-2000 | 1:50-200 |
Product Details
PNMT Antibody (YA7151) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to PNMT.
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Host Rabbit
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Clonality Recombinant
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Species ReactivityHuman Predicted Reactivity: MouseNote: The predicted reactivity is for reference only and should not be considered a guarantee of product performance.
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Observed Molecular WeightObserved band size: 30kDaNote: Due to possible protein modifications or aggregation, the molecular weight should be confirmed by actual measurement, and the predicted value is for reference only.
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Calculated Molecular Weight Predicted band size: 31kDa
A synthesized peptide derived from human PNMTase: 201-282.
Endogenous
affinity purified by Protein A
Non-conjugated
Unmodified
IgG
Product Properties
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Appearance
Solution
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Formulation
Supplied in 10mM phosphate buffered saline(pH 7.4) with 150mM sodium chloride, 0.05% BSA, 0.02% Proclin300 and 50% glycerol.
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Concentration
Batch-dependent, Please check the COA for the concentration of each lot. Check Lot Concentration
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Storage & Stability
Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.
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Shipping
Shipping with blue ice.
Background
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Function
Phenylethanolamine N-methyltransferase (PNMT) is the terminal enzyme in the catecholamine biosynthetic pathway and catalyzes the methylation of norepinephrine to form epinephrine using S-adenosyl-L-methionine as the methyl donor[1][2]. PNMT therefore serves as a key determinant of epinephrine production and contributes directly to the regulation of sympathoadrenal responses to physiological stress[1][3]. Mechanistically, PNMT expression and activity are tightly controlled by hormonal and neural inputs, with glucocorticoids from the adrenal cortex providing a major regulatory signal that induces PNMT expression in adrenal medullary chromaffin cells[3][4]. This adrenal glucocorticoid-PNMT axis supports stress-associated increases in epinephrine biosynthesis and represents a central mechanism linking endocrine and autonomic regulation[3][4]. In disease-related research, genetic variation in PNMT has been associated with altered clinical phenotypes, including pain-related outcomes in sickle cell disease and susceptibility to early-onset Alzheimer disease, highlighting the importance of epinephrine biosynthesis in human pathophysiology[5][6]. Compared with other methyltransferases involved in catecholamine metabolism, such as catechol-O-methyltransferase (COMT), PNMT performs the final biosynthetic step that generates biologically active epinephrine rather than catecholamine inactivation, making it functionally distinct within catecholamine pathways[7]. For experimental applications, selective PNMT inhibitors have been widely used to reduce epinephrine synthesis and investigate adrenergic regulation in cardiovascular, neuroendocrine, and metabolic models[7][8].
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Isoforms & Post-Translational Modification
P11086: 282 amino acids, molecular weight 30855 Da.
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SwissProt ID
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Synonyms
PENT, PNMT, Phenylethanolamine N-methyltransferase, PNMTase, Noradrenaline N-methyltransferase
Documentation
References
[1]. Betito K, et al. Adrenal phenylethanolamine N-methyltransferase induction in relation to glucocorticoid receptor dynamics: evidence that acute exposure to high cortisol levels is sufficient to induce the enzyme. J Neurochem. 1992 May;58(5):1853-62. [Content Brief]
[2]. Sadhu N, et al. Phenylethanolamine N-methyltransferase gene polymorphisms associate with crisis pain in sickle cell disease patients. Pharmacogenomics. 2020 Mar;21(4):269-278. [Content Brief]
[3]. Latuszyńska J, et al. Neurotoxic effect of dermally-applied chlorpyrifos and cypermethrin in Wistar rats. Ann Agric Environ Med. 2001;8(2):163-70. [Content Brief]