Serum creatinine detection reagent ball and serum creatinine detection chip
A detection reagent and detection chip technology, applied in measurement devices, color/spectral property measurement, material analysis by observing the influence on chemical indicators, etc. Anti-interference ability, high precision effect
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[0052] In some embodiments, the preparation method of the reagent ball (the second reagent ball or the third reagent ball) comprises the following steps:
[0053] S11. Drop the droplet of the first reagent (the second reagent or the third reagent) in liquid nitrogen, so that the droplet of the first reagent (the second reagent or the third reagent) forms an ice ball;
[0054] For example, the droplet of the first reagent (the second reagent or the third reagent) can be dropped in liquid nitrogen through a glue dispenser, so that the droplet condenses into an ice ball in the liquid nitrogen. Those skilled in the art can adjust the size of the droplet dropped into the liquid nitrogen according to actual needs, and adjust the volume of the ice puck by controlling the size of the droplet. Optionally, in some embodiments, the volume of the ice ball is 2.5-3.5 μl, for example, it may be 2.5 μl, 3 μl or 3.5 μl.
[0055] S12. Freeze-drying the ice balls to obtain freeze-dried reagent...
Embodiment 1
[0067] The raw materials of the blood creatinine detection reagent ball in this embodiment include the following components:
[0068] Each component of the first reagent is as follows: the HEPES damping fluid of 20mmol / L, the sodium chloride of 10g / L, the 2,4,6-tribromo-3-hydroxybenzoic acid of 40g / L, the Tween of 10g / L -20, 30g / L fructose, 500KU / L creatinase, 60KU / L sarcosine oxidase, 100KU / L ascorbate oxidase and 150g / L trehalose;
[0069] The components of the second reagent are as follows: 100mmol / L HEPES buffer, 5g / L sodium chloride, 0.2g / L 4-aminoantipyridine, 1g / L potassium ferrocyanide, 0.5g The Tween-20 of / L, the bovine serum albumin of 50g / L, the peroxidase of 50KU / L and the trehalose of 200g / L;
[0070] The third reagent: 1kg / L of the second reagent and 200KU / L of creatinase.
[0071] In this embodiment, the above-mentioned preparation method of blood creatinine detection reagent balls is used to prepare freeze-dried reagent balls, and the volumes of the first re...
Embodiment 2
[0074] The difference between this embodiment and embodiment 1 is as follows:
[0075] The components of the first reagent are as follows: 100mmol / L phosphate buffer, 6g / L sodium chloride, 30g / L 2,4,6-tribromo-3-hydroxybenzoic acid, 0.1g / L Triton X-100, 40g / L glycerin, 100KU / L creatinase, 200KU / L sarcosine oxidase, 50KU / L ascorbate oxidase and 200g / L water-soluble starch;
[0076] The components of the second reagent are as follows: 20mmol / L 3-morpholine propanesulfonic acid buffer, 10g / L sodium chloride, 10g / L 4-aminoantipyridine, 0.005g / L Red pigment disruptor, 10g / L Triton X-100, 10g / L glycerin, 200KU / L peroxidase and 100g / L water-soluble starch;
[0077] The third reagent: 1kg / L of the second reagent and 500KU / L of creatinase.
[0078] The volumes of the first reagent ball, the second reagent ball and the third reagent ball are about 2.5ul.
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