Serum glucose detection reagent
A technology for detecting reagents and glucose, applied in the field of glucose detection, can solve the problems of poor stability of ATP and related enzymes, and achieve the effects of enhancing anti-interference ability, high thermodynamics, and improving activity and stability
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[0048] A serum glucose detection reagent is composed of reagent R1 and reagent R2;
[0049] The reagent R1 is composed of the following components:
[0050] Buffer 100mmol / L
[0051] Mg 2+ 5mmol / L
[0052] Adenosine triphosphate (ATP) 2mmol / L
[0053] NAD+3mmol / L
[0054] Non-ionic fluorocarbon surfactant 3ml / L
[0055] BSA2g / L
[0056] Sucrose 20g / L
[0057] Trehalose 5g / L
[0058] Mannitol 20g / L
[0059] NaN 3 0.5g / L;
[0060] Described reagent R2 is made up of the composition of following content:
[0061] Buffer 100mmol / L
[0062] Mg 2+ 5mmol / L
[0063] BSA2g / L
[0064] Sucrose 20g / L
[0065] Trehalose 5g / L
[0066] Mannitol 20g / L
[0067] Glucose-6-phosphate dehydrogenase 2KU / L
[0068] Hexokinase 2KU / L
[0069] Fluorocarbon surfactant 3ml / L
[0070] NaN 3 0.5g / L.
[0071] Said, the volume ratio of R1 reagent and R2 reagent is 4:1.
[0072] Said buffer is piperazine-1,4-diethanesulfonic acid buffer at pH 7.5 at 25°C.
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