nNOS Antibody (YA7193)
(Synonyms: Nitric oxide synthase 1, Constitutive NOS, NC-NOS, NOS type I, Neuronal NOS, Peptidyl-cysteine S-nitrosylase NOS1, N-NOS, nNOS, bNOS, NOS1)Based on 1 Customer Validation
nNOS Antibody (YA7193) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to nNOS.
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Host:
Rabbit
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Isotype:
IgG
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Application:
WB
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Reactivity :
Rat
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Formulation:
Supplied in 0.01M tris buffered saline (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
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Conjugation:
Non-conjugated
Applications
| Application |
WB
WB: Western Blot
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|---|---|
| Dilution Ratio | 1:500-1:1000 |
Product Details
nNOS Antibody (YA7193) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to nNOS.
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Host Rabbit
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Clonality Recombinant,Monoclonal
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Species ReactivityRat Predicted Reactivity: Human,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: 165 kDaNote: 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: 130 kDa
KLH conjugated synthetic peptide derived from human nNOS
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 0.01M tris buffered saline (pH7.4) with 1% 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
Neuronal nitric oxide synthase (nNOS, NOS1) is a constitutively expressed nitric oxide synthase isoform that catalyzes nitric oxide (NO) production from L-arginine and functions as a major signaling enzyme in the central and peripheral nervous systems[1][2]. Mechanistically, nNOS-derived NO participates in synaptic plasticity, long-term potentiation, and neuron-to-neuron communication through NO-dependent signaling pathways, thereby contributing to learning, memory, and neural network regulation[2][3]. Beyond the nervous system, nNOS is also expressed in vascular tissues and contributes to cardiovascular homeostasis, vascular relaxation, and blood pressure regulation, indicating broader physiological functions than originally recognized[4]. In disease-related contexts, dysregulated nNOS activity has been implicated in ischemic brain injury, neurodegenerative disorders, demyelination, and other conditions associated with excessive nitric oxide and reactive nitrogen species production[3][5]. Compared with the related nitric oxide synthase isoforms, eNOS (NOS3) primarily regulates endothelial vascular function, whereas iNOS (NOS2) is inducible during inflammatory responses and generates substantially larger amounts of NO; in contrast, nNOS is calcium/calmodulin-dependent and mainly mediates physiological signaling processes[1][2][4]. For experimental applications, selective nNOS inhibitors such as 7-nitroindazole (7-NI) have been widely used to investigate nNOS-specific functions and have demonstrated neuroprotective effects in animal models of ischemic and neurotoxic injury, making them valuable pharmacological tools for mechanistic studies[6][7].
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Subcellular Localization
Cell membrane, sarcolemma,Cell projection, dendritic spine
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Expression
Tissue_Specificity: Isoform 1 is ubiquitously expressed: detected in skeletal muscle and brain, also in testis, lung and kidney, and at low levels in heart, adrenal gland and retina. Not detected in the platelets. Isoform 3 is expressed only in testis. Isoform 4 is detected in testis, skeletal muscle, lung, and kidney, at low levels in the brain, but not in the heart and adrenal gland -
Isoforms & Post-Translational Modification
P29475 has 5 isomers: P29475-1: 160970 Da (predicted); P29475-2: 148919 Da (predicted); P29475-3: 125113 Da (predicted); P29475-4: 43838 Da (predicted); P29475-5: 164779 Da (predicted).
Ubiquitinated; mediated by STUB1/CHIP in the presence of Hsp70 and Hsp40 (in vitro) -
Subunit
Homodimer
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SwissProt ID
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Synonyms
Nitric oxide synthase 1, Constitutive NOS, NC-NOS, NOS type I, Neuronal NOS, Peptidyl-cysteine S-nitrosylase NOS1, N-NOS, nNOS, bNOS, NOS1
Documentation
References
[1]. Costa ED, et al. Neuronal Nitric Oxide Synthase in Vascular Physiology and Diseases. Front Physiol. 2016 Jun 2;7:206. [Content Brief]
[2]. McMurray JJ, et al. ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: The Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESC. Eur Heart J. 2012 Jul;33(14):1787-847. [Content Brief]
[4]. 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]
[5]. Khalili M, et al. Underserved Does Not Mean Undeserved: Unfurling the HCV Care in the Safety Net. Dig Dis Sci. 2018 Dec;63(12):3250-3252. [Content Brief]
[6]. Nanri K, et al. The selective inhibitor of neuronal nitric oxide synthase, 7-nitroindazole, reduces the delayed neuronal damage due to forebrain ischemia in rats. Stroke. 1998 Jun;29(6):1248-53; discussion 1253-4. [Content Brief]
[7]. Castagnoli K, et al. The neuronal nitric oxide synthase inhibitor 7-nitroindazole also inhibits the monoamine oxidase-B-catalyzed oxidation of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. Chem Res Toxicol. 1997 Apr;10(4):364-8. [Content Brief]