Human FAAH Matched Antibody Pair Set [ABP-Q-0606] (CAT#: ABP-Q-0606)

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Human FAAH Matched Antibody Pair set for ELISA useCapture Antibody: Mouse monoclonal anti-FAAH, IgG1 KappaDetection Antibody: Mouse monoclonal anti-FAAH, IgG1 Kappa

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Antigen Detail

TargetFAAH
DescriptionFatty acid amide hydrolase or FAAH is a member of the serine hydrolase family of enzymes. It was first shown to break down anandamide in 1993. In humans, it is encoded by the gene FAAH and mainly present in the pancreas, brain, kidney, skeletal muscle, and placenta. FAAH is a promising target for treating many disease conditions including pain, inflammation and mood disorders.
Species ReactivityHuman

Capture Antibody

Capture ClonalityMonoclonal
Host SpeciesMouse
CloneIV01785
IsotypeIgG1, kappa
PurificationAffinity chromatography
BufferPBS, pH 7.4, containing 0.1% Proclin 300
ApplicationELISA

Detection Antibody

Det-ClonalityMonoclonal
Host SpeciesMouse
ConjugationBiotin
CloneRD10231
IsotypeIgG1, kappa
PurificationAffinity chromatography
BufferPBS, pH 7.4

General Product Property

Product OverviewHuman FAAH Matched Antibody Pair set for ELISA use
Capture Antibody: Mouse monoclonal anti-FAAH, IgG1 Kappa
Detection Antibody: Mouse monoclonal anti-FAAH, IgG1 Kappa
SpecificityValidated for detecting natural and recombinant human FAAH
Research AreaNeurotransmission
ApplicationELISA
Application NotesOptimal dilutions should be determined experimentally by the user.
FormLyophilized
StorageAvoid repeated freeze/thaw cycles. Store at 2-8°C for short term. Aliquot and store at -20°C for long term storage.
Size1 Set
Sample TypeSerum; Supernatant; Urine; Cell lysate; Plasma; Tissue Homogenates
Usage StatementAvailable for Research Use Only. Not for use in therapeutic or diagnostic applications.

Target Overview

Gene SymbolFAAH
Full NameFatty Acid Amide Hydrolase
BackgroundThis gene encodes a protein that is responsible for the hydrolysis of a number of primary and secondary fatty acid amides, including the neuromodulatory compounds anandamide and oleamide.
Alternative NamesPSAB
Gene ID2166
Uniprot IDO00519
HGNC3553
EnsemblENSG00000117480
OMIM602935
Involvement in DiseaseDiseases associated with FAAH include Polysubstance Abuse and Cannabis Dependence.
FunctionCatalyzes the hydrolysis of endogenous amidated lipids like the sleep-inducing lipid oleamide ((9Z)-octadecenamide), the endocannabinoid anandamide (N-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-ethanolamine), as well as other fatty amides, to their corresponding fatty acids, thereby regulating the signaling functions of these molecules (PubMed:9122178, PubMed:17015445, PubMed:19926788). Hydrolyzes polyunsaturated substrate anandamide preferentially as compared to monounsaturated substrates (PubMed:9122178, PubMed:17015445). Also catalyzes the hydrolysis of the endocannabinoid 2-arachidonoylglycerol (2-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-glycerol) (PubMed:21049984).
Related PathwaysIts related pathways are GABAergic synapse and Arachidonic acid metabolism.

For Research Use Only.

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