Anti-interference and stable serum direct bilirubin (enzymatic method) determination kit as well as preparation method and application thereof
A technology of bilirubin oxidase and kit, which is applied in the field of direct bilirubin assay kit preparation and direct bilirubin assay kit, and can solve the problems of poor anti-interference ability, influence, and easy contamination of instruments, etc.
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[0051] A conventional direct bilirubin assay kit, which includes reagent R1 and reagent R2.
[0052] Reagent R1 contains the following components:
[0053] Phosphate buffer 25mmol / L;
[0054] NaCl 1g / L;
[0055] N-acetylcysteine 1g / L;
[0056] Sodium fluoride 0.1g / L;
[0057] Disodium EDTA 0.1g / L;
[0058] Ascorbate oxidase 1KU / L;
[0059] Sorbitan Laurate 1%;
[0060] Polyoxypropylene mannitol dioleate 1%;
[0061] proclin300 1 ml / L.
[0062] The pH of reagent R1 is 5.2.
[0063] Reagent R2 contains the following components:
[0064] Piperazine-1,4-diethanesulfonic acid (PIPES) buffer 50mmol / L;
[0065] Bovine Serum Albumin (BSA) 5g / L;
[0066] Mannitol 10g / L;
[0067] Triton 100 1%;
[0068] Bilirubin oxidase 1KU / L;
[0069] proclin300 1ml / L.
[0070] The pH of reagent R2 is 9.0.
[0071] Wherein the percentages are volume ratios.
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