Stable liquid kit for measuring lactic acid
A technology of kits and reagents, applied in the field of medical testing and determination, can solve the problems such as the decrease of pH value of reagents, poor stability of reagents when opening bottles, and stability of reagents affecting the accuracy of measurement, and achieve the effect of promoting the reaction.
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Embodiment 1
[0030] The components and concentrations of reagent 1 are:
[0031] Imidazole buffer (pH 5.5) 0.3 M
[0032] α-Naphthol 20 mg / L
[0033] NAD 20 mg / L
[0034] Sodium azide 0.2 g / L
[0035] The components and concentrations of reagent 2 are:
[0036] Piperazine-1,4-diethanesulfonic acid buffer (pH 8.5) 0.1M
[0037] Lactate dehydrogenase 50 KU / L
[0038] Ethylene glycol 10 g / L
[0039] Proclin300 0.5 g / L.
[0040] The preparation method of Reagent 1 and Reagent 2 is a conventional method, that is, the components of Reagent 1 and Reagent 2 are added to distilled water and then mixed and stirred evenly.
Embodiment 2
[0042] The components and concentrations of reagent 1 are:
[0043] Citric acid-trisodium citrate buffer (pH 6.0) 0.1 M
[0044] β-Naphthol 20 mg / L
[0045] thio-NAD 50 mg / L
[0046] Proclin300 0.1 g / L
[0047] The components and concentrations of reagent 2 are:
[0048] Tris buffer (pH 9.0) 0.2 M
[0049] Lactate dehydrogenase 80 KU / L
[0050] Bovine serum albumin 0.1 g / L
[0051] Proclin300 1 g / L
[0052] The preparation method of the kit of Example 2 is the same as that of Example 1.
Embodiment 3
[0064] Example 3 The preparation method of the kit is the same as in Example 1.
[0065] The test conditions for determining the lactic acid in the sample by the kit of the present invention are as follows: temperature: 30-37°C; and the optical path of the cuvette is 1.0 cm. The main wavelength of detection is 340 nm and the secondary wavelength is 405 nm.
[0066] The method of using the lactic acid determination kit of the present invention to determine lactic acid in a sample is as follows: the sample (calibration tube uses the calibrator as the sample) is mixed with R1, the absorbance A0 is read after incubating at 30-37°C for 3-5 min, and R2 is added immediately to mix. After reacting at 30-37°C for 5 minutes, read the absorbance A1, ΔA=A1-A0. The sample volume is 3 μl, the reagent 1 volume is 200 μl, and the reagent 2 volume is 50 μl.
[0067] The LAC content in the sample determined by the kit of the present invention is calculated according to the following formula:
[0068]...
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