NNMT Antibody (YA7772)
(Synonyms: nicotinamide N-methyltransferase)NNMT Antibody (YA7772) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to NNMT.
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Host:
Mouse
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Isotype:
IgG
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Application:
IHC-P, ICC/IF, FC
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Reactivity :
Human, Dog, Mouse, Rat
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Formulation:
Spplied in PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
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Conjugation:
Non-conjugated
Applications
| Application |
IHC-P
IHC-P: Immunohistochemistry-Paraffin
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ICC/IF
ICC/IF: Immunocytochemistry/
Immunofluorescence |
FC
FC: Flow Cytometry
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|---|---|---|---|
| Dilution Ratio | 1:150-500 | 1:100-250 | 1:100 |
Product Details
NNMT Antibody (YA7772) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to NNMT.
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Host Mouse
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Clonality Monoclonal
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Species ReactivityHuman, Dog, Mouse, Rat
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Calculated Molecular Weight Predicted band size: 29.4 kDa
Full length human recombinant protein of human NNMT produced in HEK293T cell.
Endogenous
Affinity purified
Non-conjugated
Unmodified
IgG
Product Properties
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Appearance
Solution
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Formulation
Spplied in PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
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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
NNMT (nicotinamide N-methyltransferase) is a cytosolic methyltransferase that transfers a methyl group from S-adenosylmethionine (SAM) to nicotinamide (NAM), generating 1-methylnicotinamide (1-MNA) and S-adenosylhomocysteine (SAH), thereby connecting NAD+ metabolism with cellular methyl-donor utilization[1][2]. Mechanistically, NNMT regulates metabolic homeostasis by influencing intracellular SAM availability, NAD+ salvage, and methylation potential, which positions the enzyme at the intersection of energy metabolism and epigenetic control[1][3][4]. NNMT-driven consumption of methyl donors can create a metabolic methylation sink that remodels histone methylation patterns and alters gene-expression programs in cancer cells[3]. In disease models, elevated NNMT expression has been associated with obesity, metabolic dysfunction, fibrosis, and multiple malignancies, whereas genetic or pharmacological suppression of NNMT improves metabolic phenotypes and modifies disease progression pathways[4][5][6]. Compared with related methyltransferases such as GNMT (glycine N-methyltransferase), which primarily regulates systemic SAM/SAH balance through glycine methylation, NNMT directly links NAM turnover to NAD+ and one-carbon metabolism, giving it a distinct role in metabolic reprogramming[2][7]. For experimental applications, selective small-molecule NNMT inhibitors and bisubstrate analogs have been developed as chemical probes to evaluate target engagement, metabolic remodeling, and therapeutic responses in cancer and metabolic disease models[6][8].
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Subcellular Localization
Cytoplasm
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Expression
Tissue_Specificity: Predominantly expressed in the liver. A lower expression is seen in the kidney, lung, skeletal muscle, placenta and heart. Not detected in the brain or pancreas -
Isoforms & Post-Translational Modification
P40261: 264 amino acids, molecular weight 29574 Da.
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Subunit
Monomer
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SwissProt ID
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Synonyms
nicotinamide N-methyltransferase
Documentation
[1]. Pissios P. Nicotinamide N-Methyltransferase: More Than a Vitamin B3 Clearance Enzyme. Trends Endocrinol Metab. 2017 May;28(5):340-353. doi: 10.1016/j.tem.2017.02.004. Epub 2017 Mar 11. PMID: 28291578; PMCID: PMC5446048. et al. Nicotinamide N-Methyltransferase: More Than a Vitamin B3 Clearance Enzyme. Trends Endocrinol Metab. 2017 May;28(5):340-353. [Content Brief]
[2]. Rabezanahary H, et al. Live virus neutralizing antibodies against pre and post Omicron strains in food and retail workers in Québec, Canada. Heliyon. 2024 May 21;10(10):e31026. [Content Brief]
[3]. Kiros M, et al. Trends in HIV-1 pretreatment drug resistance and HIV-1 variant dynamics among antiretroviral therapy-naive Ethiopians from 2003 to 2018: a pooled sequence analysis. Virol J. 2023 Oct 25;20(1):243. [Content Brief]
[4]. Kraus D, et al. Nicotinamide N-methyltransferase knockdown protects against diet-induced obesity. Nature. 2014 Apr 10;508(7495):258-62. [Content Brief]
[5]. Wang W, et al. Complex roles of nicotinamide N-methyltransferase in cancer progression. Cell Death Dis. 2022 Mar 25;13(3):267. [Content Brief]
[6]. Treherne JM, et al. Converging global crises are forcing the rapid adoption of disruptive changes in drug discovery. Drug Discov Today. 2021 Nov;26(11):2489-2495. [Content Brief]
[7]. Wikipedia.
[8]. Deng Y, et al. Semisynthesis of Platensimycin Derivatives with Antibiotic Activities in Mice via Suzuki-Miyaura Cross-Coupling Reactions. J Med Chem. 2018 Dec 27;61(24):11341-11348. [Content Brief]