Enzymatic method detection kit of D-3-hydroxybutyric acid and preparation method thereof
A D-3-, kit technology, applied in the direction of biochemical equipment and methods, biological testing, material inspection products, etc., can solve the problems of long operation time of capillary isotachophoresis, unacceptable chemical substances, difficult to use in large quantities, etc. Achieve the effect of great clinical application value, stability improvement and strong protective effect
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Embodiment 1
[0034] Example 1 Preparation of D-3-hydroxybutyric acid detection kit
[0035] composition:
[0036] Reagent 1: (3L) (reagent volume)
[0037]
[0038] Reagent 2: (1L) (reagent volume)
[0039]
[0040] preparation:
[0041] (1) Preparation of reagent 1: (3L)
[0042] (1) First add 2.4L of deionized water to the container;
[0043] (2) Add tris buffer, polyoxypropylene polyoxyethylene copolymer (F108), and sodium azide in sequence;
[0044] (3) Add enzyme: D-3-hydroxybutyrate dehydrogenase
[0045] (4) Finally, add deionized water to a total volume of 3L and mix evenly to obtain;
[0046] (2) Preparation of reagent 2: (1L)
[0047] Add oxalate, oxidized coenzyme, and sodium azide deionized water to the container in sequence until the total volume is 1 L, and mix well.
Embodiment 2
[0049] Reagent 1: (3L) (reagent volume)
[0050]
[0051] Reagent 2: (1L) (reagent volume)
[0052] Oxalate 3.5g
[0053] Oxidized Coenzyme 3g
[0054] Sodium azide 1g
[0055] Deionized water was added to a total volume of 1 L.
[0056] The preparation method is the same as in Example 1.
Embodiment 3
[0058] Reagent 1: (3L) (reagent volume)
[0059]
[0060] Reagent 2: (1L) (reagent volume)
[0061] Oxalate 5g
[0062] Oxidized coenzyme 3g
[0063]Sodium azide 1g
[0064] Deionized water was added to a total volume of 1 L.
[0065] Preparation method is the same as embodiment 1
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