Inorganic phosphorus detection reagent and detection chip
A detection reagent and detection chip technology, applied in measurement devices, color/spectral property measurement, material analysis by observing the impact on chemical indicators, etc., can solve problems such as poor anti-interference ability, and achieve strong anti-interference ability. Effect
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[0056] The embodiment of the present invention also provides a preparation method of an inorganic phosphorus detection reagent, the method comprising the following steps:
[0057] S11. Acquiring reagents, the first reagent and the second reagent;
[0058] In some embodiments, the configuration process of the first reagent is as follows: add an appropriate amount of distilled water into the container, weigh the buffer components, add maltose and oxidized coenzyme in turn after the buffer solution is completely dissolved, and adjust the pH to 6.5-7.5, Finally, the excipient is added, and then the volume is constant to obtain the first reagent. In some embodiments, the configuration process of the second reagent is as follows: add an appropriate amount of distilled water into the container, weigh the buffer components, and add β-glucomutase, maltose phosphorylase, and Glucose-6-phosphate dehydrogenase, adjust the pH to 6.5-7.5, finally add excipients, and then adjust the volume ...
Embodiment 1
[0066] The raw material components of the inorganic phosphorus detection reagent in the inorganic phosphorus detection chip provided in this embodiment include:
[0067] The components of the first reagent are as follows:
[0068] PIPES buffer 20mmol / L;
[0069] EDTA 1g / L;
[0070] Glycerin 10g / L;
[0071] Maltose 50g / L;
[0072] Oxidized coenzyme I 20L;
[0073] Trehalose 100g / L;
[0074] The pH value of the first reagent was 6.7.
[0075] The components of the second reagent are as follows:
[0076] PIPES buffer 100mmol / L;
[0077] EDTA 10g / L;
[0078] β-glucomutase phosphate 10KU / L;
[0079] Maltose phosphorylase 10KU / L;
[0080] Glucose-6-phosphate dehydrogenase 20KU / L;
[0081] Trehalose 150g / L;
[0082] Dextran 10,000 50g / L;
[0083] The pH of the second reagent was 6.7.
Embodiment 2
[0085] The difference between this embodiment and embodiment 1 is as follows:
[0086] The components of the first reagent are as follows:
[0087] Bis-Tris buffer 100mmol / L;
[0088] Bovine serum albumin 10g / L;
[0089] Maltose 25g / L;
[0090] Oxidized coenzyme II 50g / L;
[0091] Mannitol 120g / L;
[0092] The pH of the first reagent was 7.0.
[0093] The components of the second reagent are as follows:
[0094] Bis-Tris buffer 100mmol / L;
[0095] Bovine serum albumin 1g / L;
[0096] β-glucomutase phosphate 20KU / L;
[0097] Maltose phosphorylase 20KU / L;
[0098] Glucose-6-phosphate dehydrogenase 40KU / L;
[0099] Dextran 40,000 50g / L;
[0100] Mannitol 80g / L;
[0101] The pH of the second reagent was 7.0.
[0102] The performance of the inorganic phosphorus detection chip obtained in Example 1 of the present invention will be described below in conjunction with the table. It should be noted that, at 37° C., the change value of the absorbance of the assay chip injec...
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