Kit of detecting D-3-hydroxybutyric acid through enzymic method and preparation method thereof
A D-3-, kit technology, applied in biochemical equipment and methods, microbial determination/inspection, etc., can solve the problems of bilirubin interference, influence detection, negative values, etc., and achieve anti-bilirubin interference. The performance enhancement, the clinical application value and the sensitivity improvement effect
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2016-07-06
Smart Images
Figure 1 Figure 2 Figure 3
Abstract
Description
technical field
[0001] The invention relates to biological reagents, in particular to a detection kit, in particular to a kit for enzymatic detection of D-3-hydroxybutyric acid and a preparation method thereof. Background technique
[0002] Diabetic ketoacidosis is a common clinical disease, frequently-occurring disease, caused by increased blood ketones, D-3-hydroxybutyric acid is the main component of ketones in the blood (accounting for 78%), it can reflect the ketones in the blood generated situation. When ketoacidosis occurs, D-3-hydroxybutyric acid is significantly increased. Therefore, D-3-hydroxybutyric acid can be used for early diagnosis and treatment monitoring of ketoacidosis, and can guide the treatment and efficacy monitoring of ketoacidosis . Because in ketoacidosis, the patient has an antagonistic effect on insulin, resulting in protein synthesis disorder and protein degradation metabolism, therefore, by measuring the fasting blood sugar in the morning, it ...
Examples
Embodiment 1
[0028] Example 1 Preparation of D-3-hydroxybutyric acid detection kit
[0029] composition:
[0030] Reagent 1: (3L) (reagent volume)
[0031]
[0032] Reagent 2: (1L) (reagent volume)
[0033]
[0034]
[0035] preparation:
[0036] (1) Preparation of reagent 1: (3L)
[0037] (1) First add 2.4L of deionized water to the container;
[0038] (2) Tris buffer solution, lauryl polyethylene glycol ether, sodium azide are added successively;
[0039] (3) Add enzyme: D-3-hydroxybutyrate dehydrogenase
[0040] (4) Finally, add deionized water until the total volume is 3L and mix evenly to obtain;
[0041] (2) Preparation of reagent 2: (1L)
[0042] Add oxalate, 3-acetylpyridine oxidized coenzyme, and sodium azide deionized water to the container in sequence until the total volume is 1 L, and mix well.
Embodiment 2
[0044] Reagent 1: (3L) (reagent volume)
[0045]
[0046] Reagent 2: (1L) (reagent volume)
[0047]
[0048]
[0049] The preparation method is the same as in Example 1.
Embodiment 3
[0051] Reagent 1: (3L) (reagent volume)
[0052]
[0053] Reagent 2: (1L) (reagent volume)
[0054]
[0055] Preparation method is the same as embodiment 1