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96T $ 450.00
48T $ 300.00
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For research use only.

Detection Principle Free fatty acids produce acyl coenzyme A in the presence of acyl synthase, which produces hydrogen peroxide in the presence of acyl oxidase. In the presence of the enzyme and probe, hydrogen peroxide react to produce the fluorescence substrate. The fluorescence intensity at the excitation wavelength of 535 nm and emission wavelength of 590 nm is directly proportional to the concentration of free fatty acids.
Synonyms FFA;NEFA
Sample Type Serum,Plasma,Animal tissue,Cell
Detection Method Fluorometric method
Detection Instrument Fluorescence microplate reader (Ex/Em=535 nm/590 nm)
Research Area Metabolic Diseases ,  Glycolysis And Lipid Metabolism ,  Energy Metabolism
Storage This product can be stored at -20°C for 12 months with shading light.
Valid Period 12 months
Sensitivity 1.20 μmol/L
Detection Range 1.20-100 μmol/L
Precision inter-assay CV: 5.1% | intra-assay CV: 4.1%
Sample Volume 50 μL
Assay Time 1 h 10 min

The recommended dilution factor for different samples is as follows (for reference only):

Sample Type Dilution Factor
Human serum 10-20
Rat serum 200-400
Mouse plasma 100-300
Rabbit serum 100-300
10% Rat liver tissue homogenate 200-400
10% Mouse kidney tissue homogenate 200-400
10% Rat brain tissue homogenate 200-400
10% Rat lung tissue homogenate 200-400

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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