Free fatty acid determining kit and preparation method thereof
A free fatty acid and kit technology, applied in biochemical equipment and methods, microbial measurement/inspection, etc., can solve the problems of large enzyme usage, short storage time, and easy interference of enzyme activity by various factors. Achieve rapid filtration, easy filtration, and slow down denaturation
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Embodiment 1
[0023]
[0024]
[0025] Reagent R1 preparation method: take 800mL of water, add sodium dihydrogen phosphate to 50mmol / L, fully dissolve, adjust the pH to 7.2 with NaOH, add coenzyme A to 0.05mmol / L, ATP to 3mmol / L, ACS to 0.4KU / L, MgCl 2 to 2mmol / L, Trinder substrate to 0.5g / L
[0026] Reagent R2 preparation method: take 800mL of water, add sodium dihydrogen phosphate to 60mmol / L, fully dissolve, adjust pH to 7.2 with NaOH, add FAD to 2mmol / L, 4-AA to 10mmol / L, ACOD to 40KU / L L. Tween 20 to <1%, glycerol to 20%-30%, Brj35 to 1-1.5g / L, EDTA-2Na to 1g / L.
Embodiment 2
[0028]
[0029]
[0030] The preparation method is the same as in Example 1.
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