Kit for detecting 1, 5-AG with good stability and method
A detection kit, 5-AG technology, applied in 1 field, can solve the problems of weakened ability to eliminate glucose, poor stability of HK enzyme, poor stability of 1,5-AG detection kit, etc., to achieve good stability, The effect of high accuracy and precision and strong anti-glucose interference ability
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Embodiment 1
[0030] Preparation process of 1,5-AG detection kit in serum:
[0031] Composition and concentration of reagent R1:
[0032] MES (pH6.0) 50mmol / L
[0033] Hexokinase 15KU / L
[0034] Pyruvate kinase 10KU / L
[0035] ATP 5mmol / L
[0036] 4-Aminoantipyridine 3mmol / L
[0037] Phosphoenolpyruvate 3mmol / L
[0038] Triton X-100 5g / L
[0039] WD-001 5g / L
[0040] Magnesium chloride 6mmol / L
[0041] Proclin300 5g / L;
[0042] Composition and concentration of reagent R1:
[0043] HEPES (pH7.5) 50mmol / L
[0044] Pyranose oxidase 50KU / L
[0045] Peroxidase 20KU / L
[0046] p-Hydroxybenzoic acid 10mmol / L
[0047] Proclin300 5g / L
[0048] Triton X-100 5g / L.
[0049] Application of 1,5-AG detection kit in serum on automatic biochemical analyzer:
[0050] Analysis method: two-point endpoint method
[0051] Reaction Direction: Rising Reaction
[0052] Calibration method: line
[0053] Determination of dominant wavelength: 546nm
[0054] Determination of sub-wavelength: 700nm
[...
Embodiment 2
[0060] 1,5-AG assay kit performance evaluation
[0061] 1. Analytical sensitivity
[0062] The kit B of the present invention prepared in Example 1 and the commercially available 1,5-AG assay kit A were calibrated simultaneously with their respective calibrators, and the results are shown in Table 1.
[0063] Table 1 1,5-AG assay kits on sale and calibration results of the kits of the present invention
[0064]
[0065] As can be seen from Table 1, when the 1,5-AG content of the kit B of the present invention is 150 μmol / L, the absorbance change rate is 0.0572, and when the 1,5-AG content of the kit A on sale is 150 μmol / L, the absorbance The rate of change is 0.0330, which shows that the analytical sensitivity of the kit B of the present invention is significantly higher than that of the commercially available kit A.
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