Composition and application thereof in detecting activity of lipoprotein-associated phospholipase A2
A composition and lipoprotein technology, applied in the field of medical testing, can solve the problems of reduced substrate stability, inconvenient use, influence on reagent blank absorbance and reagent validity period, etc.
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Embodiment 1
[0065] The detection reagent combination of the present embodiment comprises:
[0066] The composition of reagent 1 (or called R1 reagent, the first reagent) is as follows:
[0067] 100mmol / L 4-hydroxyethylpiperazineethanesulfonic acid (HEPES), 15mmol / L ethylenediaminetetraacetic acid (EDTA), 9mmol / L 3-[3-(cholamidopropyl)dimethylaminopropanesulfonic acid Salt (CHAPS), 10mmol / L sodium n-nonane sulfonate, 200mmol / L sodium chloride, the balance is water; the pH of reagent 1 is 7.6.
[0068] The composition of reagent 2 (or called R2 reagent, second reagent) is as follows:
[0069] 20mmol / L citric acid, 15mmol / L sodium n-nonanesulfonate, 5wt% ethanol, 3mmol / L 1-tetradecanoyl-2-4-p-nitrophenol succinic anhydride-3-phosphatidylcholyl, 0.05wt %18-Crown Ether-6, 0.1wt% Dextran 40 (also known as Dextran-40, Dextran-40, Dextran T-40, Dextran T-40), the balance is water; the pH of reagent 2 is 4.5 . The mass percent concentration mentioned in Reagent 2 refers to the mass percent con...
Embodiment 2
[0071] Lp-PLA in embodiment 2 and embodiment 1 2 The only difference in the assay kit is that the stabilizer in reagent R2 is 0.05wt% 18-crown-6, and the others are the same as those in Example 1, and will not be repeated here.
Embodiment 3
[0073] Embodiment 3 and the Lp-PLA in embodiment 1 2 The only difference in the assay kit is that the stabilizers in the reagent R2 are 0.05wt% 15-crown-5 and 0.1wt% dextran 40. Others are the same as in Example 1 and will not be repeated here.
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