Enzymatic chemiluminescence based detection kit for UA (uric acid) determination
A detection kit and luminescence technology, applied in the biological field, can solve the problems of low specificity, interference and poor stability of peroxidase, and achieve the effects of enhancing anti-interference ability, reducing interference and high sensitivity
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Embodiment 1
[0037] Embodiment 1, the preparation of Tween 80 primary degradant
[0038] Add Tween 80 solution into a 100ml shake flask, inoculate 1~3wt% Trichoderma viride with a concentration of 1000cfu / mL, set the temperature at 35°C, rotate at 120r / min, cultivate for 12h, centrifuge, and take the supernatant; Microfiltration was performed on clear water, cation exchange and sterilization were performed on 732 type cation exchange resin, and the primary degradation product of Tween 80 was obtained.
Embodiment 2
[0039] Example 2, a detection kit for the determination of uric acid by enzymatic chemiluminescence
[0040] Reagent R1:
[0041]
[0042] Reagent R2:
[0043]
[0044] Reagent R3:
[0045] Lumigen HyPerBlu.
Embodiment 3
[0046] Example 3, a detection kit for the determination of uric acid by enzymatic chemiluminescence
[0047] The difference between Example 3 and Example 2 is that the anti-interference agent I in the reagent R1 is ascorbate oxidase and potassium ferrocyanide, the concentration of the primary degradation product of Tween 80 is 0.03w / v%, and the remaining parameters and operations are as implemented Example 2 shows.
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