FAAH1 Antibody (YA2064)
(Synonyms: FA2H; FAAH; FAAH-1; Oleamide hydrolase 1; Oleamide hydrolase)Based on 1 Customer Validation
FAAH1 Antibody (YA2064) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to FAAH1.
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Host:
Rabbit
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Isotype:
IgG
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Application:
WB, IHC-P
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Reactivity :
Human, Mouse
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Formulation:
Supplied in rabbit IgG in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA.
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Conjugation:
Non-conjugated
Applications
| Application |
WB
WB: Western Blot
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IHC-P
IHC-P: Immunohistochemistry-Paraffin
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|---|---|---|
| Dilution Ratio | 1:1000-1:2000 | 1:50-1:100 |
Product Details
FAAH1 Antibody (YA2064) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to FAAH1.
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Host Rabbit
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Clonality Recombinant,Monoclonal
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Species ReactivityHuman, Mouse
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Observed Molecular WeightObserved band size: 63 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: 63 kDa
A synthesized peptide derived from human FAAH1 aa500-579/579.
Endogenous
Affinity Chromatography
Non-conjugated
Unmodified
IgG
Product Properties
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Appearance
Solution
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Formulation
Supplied in rabbit IgG in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA.
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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
FAAH-1 (fatty acid amide hydrolase-1) is a membrane-associated serine hydrolase that terminates endocannabinoid signaling by hydrolyzing anandamide and other bioactive fatty acid amides, thereby regulating their tissue concentration and biological activity[1][2]. Mechanistically, FAAH-1 functions as a major catabolic enzyme within the endocannabinoid pathway and controls the magnitude and duration of lipid-mediated signaling processes relevant to neuronal, inflammatory, and peripheral physiological responses[1][3]. Experimental studies demonstrated that loss of FAAH activity enhances endogenous cannabinoid signaling and increases sensitivity to anandamide, establishing FAAH-1 as a critical regulator of endocannabinoid homeostasis in vivo[4]. In disease-relevant and pharmacological models, modulation of FAAH activity has therefore been widely used to investigate pain, neuroinflammation, and other endocannabinoid-dependent biological processes[3][4]. Compared with the related isoform FAAH-2, FAAH-1 exhibits substantially greater catalytic activity toward N-acyl ethanolamines, including anandamide, and toward N-acyl taurines, highlighting a distinct substrate preference within fatty acid amide metabolism[5]. FAAH-1 and FAAH-2 also display overlapping but distinct tissue distributions, suggesting complementary roles in controlling fatty acid amide catabolism in primates[5]. For experimental applications, selective FAAH inhibitors such as URB597, PF-3845, and related compounds are extensively employed to elevate endogenous fatty acid amide levels and probe endocannabinoid signaling mechanisms, making FAAH-1 a well-established pharmacological target for mechanistic research[2][3].
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Subcellular Localization
Endomembrane system; Single-pass membrane protein; Cytoplasm, cytoskeleton
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Expression
Tissue_specificity:Highly expressed in the brain, small intestine, pancreas, skeletal muscle and testis. Also expressed in the kidney, liver, lung, placenta and prostate -
Subunit
Homodimer
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SwissProt ID
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Synonyms
FA2H; FAAH; FAAH-1; Oleamide hydrolase 1; Oleamide hydrolase
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Research Field
Signal Transduction
Documentation
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Data Sheet (262 KB)
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SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
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User Guide for Antibodies (1077 KB)
[1]. Dainese E, et al. The endocannabinoid hydrolase FAAH is an allosteric enzyme. Sci Rep. 2020 Feb 10;10(1):2292. [Content Brief]
[2]. van Egmond N, et al. Targeting Endocannabinoid Signaling: FAAH and MAG Lipase Inhibitors. Annu Rev Pharmacol Toxicol. 2021 Jan 6;61:441-463. [Content Brief]
[3]. Lee MJ, et al. Time to HIV rebound after infusion of long-acting broadly neutralising antibodies 3BNC117-LS and 10-1074-LS and analytical treatment interruption (the RIO trial): a double-blind, randomised, placebo-controlled trial. Lancet HIV. 2026 May 27:S2352-3018(26)00059-7. [Content Brief]
[4]. Cravatt BF, et al. Supersensitivity to anandamide and enhanced endogenous cannabinoid signaling in mice lacking fatty acid amide hydrolase. Proc Natl Acad Sci U S A. 2001 Jul 31;98(16):9371-6. [Content Brief]
[5]. Wei BQ, et al. A second fatty acid amide hydrolase with variable distribution among placental mammals. J Biol Chem. 2006 Dec 1;281(48):36569-78. [Content Brief]