Latex microspheres, application thereof and glycosylated hemoglobin detection kit
A technology of glycosylated hemoglobin and detection kits, which is applied in the direction of anti-animal/human immunoglobulin, biological testing, measuring devices, etc., can solve the problem of inaccurate testing of anemia samples, and achieve long-term storage and use, eliminate influence, and stabilize good sex effect
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Embodiment 1
[0038] Example 1: Preparation of the detection kit of the present invention
[0039] All components shown in Table 2 below were mixed at the concentrations shown below to prepare Reagent R1 and Reagent R2.
[0040] Table 2
[0041]
[0042] Detection method: Dilute the sample 100 times with hemolyzing agent, add 10uL sample, 260uL latex reagent R1, incubate at 37℃ for 30 seconds, then add antibody reagent R2, react at 37℃ for 3 minutes, and measure the absorbance value at 660nm. The percentage of HbA1c in the sample was calculated according to the standard curve of the percentage concentration of HbA1c.
Embodiment 2
[0043] Example 2: Preparation of the detection kit of the present invention
[0044] All components shown in Table 3 below were mixed at the concentrations shown below to prepare Reagent R1 and Reagent R2.
[0045] table 3
[0046]
[0047] Detection method: Dilute the sample 100 times with hemolyzing agent, add 10uL sample, 260uL latex reagent R1, incubate at 37℃ for 30 seconds, then add antibody reagent R2, react at 37℃ for 3 minutes, and measure the absorbance value at 660nm. The percentage of HbA1c in the sample was calculated according to the standard curve of the percentage concentration of HbA1c.
Embodiment 3
[0048] Example 3: Preparation of the detection kit of the present invention
[0049] All components shown in Table 4 below were mixed at the concentrations shown below to prepare Reagent R1 and Reagent R2.
[0050] Table 4
[0051]
[0052]
[0053] Detection method: Dilute the sample 100 times with hemolyzing agent, add 10uL sample, 260uL latex reagent R1, incubate at 37℃ for 30 seconds, then add antibody reagent R2, react at 37℃ for 3 minutes, and measure the absorbance value at 660nm. The percentage of HbA1c in the sample was calculated according to the standard curve of the percentage concentration of HbA1c.
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