Fatty Acid Amide Hydrolase (FAAH) Activity Fluorometric Assay Kit (E-BC-F082)
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For research use only.
Detection Principle | Fatty acid amide hydrolase (FAAH) is a membrane binding protein belonging to the serine hydrolase family. FAAH hydrolyzes many important endogenous fatty acid amides, including endocannabinoid (AEA) and palmitoyl glycolamide (PEA). FAAH plays a key role in controlling cannabinoid signaling by hydrolyzing 2-arachidenol glycerol in AEA and certain tissues. Detection principle: FAAH hydrolyzes a non-fluorescent substrate releasing a fluorophore, and detect fluorescence at the excitation wavelength of 340 nm and the emission wavelength of 440 nm. Because FAAH is a serine protein, FAAH-specific inhibitors are used in the kit to inhibit enzyme activity and exclude the effects of non-specific enzyme activity. |
Sample Type | Animal tissue,Cell |
Detection Method | Fluorometric method |
Detection Instrument | Fluorescence microplate reader (Ex/Em=340 nm/440 nm) |
Research Area | Glycolysis And Lipid Metabolism |
Storage | This product can be stored at -20°C for 12 months with shading light. |
Valid Period | 12 months |
Sensitivity | 0.004 U/L |
Detection Range | 0.004-0.105 U/L |
Precision | inter-assay CV: 0.2-12.2% | intra-assay CV: 3.7-6.0% |
Sample Volume | 40 μL(tissue/cell homogenate) |
Assay Time | 1 h |
The recommended dilution factor for different samples is as follows (for reference only):
Sample Type | Dilution Factor |
---|---|
10% Mouse liver tissue homogenate | 1 |
10% Mouse kidney tissue homogenate | 1 |
10% Mouse brain tissue homogenate | 1 |
10% Mouse lung tissue homogenate | 1 |
1×10^6 293T cells | 1 |
The diluent is normal saline (0.9% NaCl) or PBS (0.01 M, pH 7.4). For the dilution of other sample types, please do pretest to confirm the dilution factor.
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