Magnetic particle chemiluminiscence kit for measuring content of prealbumin in human body and preparation method thereof
A technology of prealbumin and chemiluminescence, which is applied in the field of magnetic particle chemiluminescence detection kit, magnetic particle chemiluminescence detection kit and its preparation, can solve the problems of low sensitivity, narrow linear range, unstable results, etc. Low processing requirements, simple operation, and the effect of ensuring sensitivity
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Embodiment 1
[0047] Example 1 Preparation of a magnetic particle chemiluminescence detection kit for measuring the content of human prealbumin
[0048] The kit includes R1 reagent, R2 reagent, magnetic separation reagent, calibrator liquid series and chemiluminescence substrate liquid.
[0049] Among them, R1 reagents include: 1) R1 antibody: Fluorescein isothiocyanate (FITC) labeled anti-human prealbumin monoclonal antibody at a concentration of 1 μg / ml; 2) buffer: including Tris at a concentration of 12.0 g / L; sodium azide, the concentration is 1.98g / L; sodium chloride, the concentration is 5.9g / L; fish skin gelatin, the concentration is 10g / L; the rest is deionized water. The buffer pH of the R1 reagent is 8.0.
[0050] Among them, the R2 reagents include: 1) R2 antibody: alkaline phosphatase-labeled anti-human prealbumin antibody at a concentration of 0.5 μg / ml; 2) buffer: a commercial AP Conjugate Stabilizer. The buffer pH of R2 reagent is 8.0.
[0051] Among them, the magnetic separation ...
Embodiment 2
[0054] Example 2 Preparation and determination method of magnetic particle chemiluminescence detection kit for measuring human prealbumin content
[0055] (1) First, compare the 50μl calibrator series (concentrations of 0mg / dL, 1.5mg / dL, 3.5mg / dL, 7mg / dL, 20mg / dL, 60mg / dL) of Example 1 with those of Example 1. Add 50μl reagent R1 and 50μl reagent R2 to the reaction tube in sequence, and incubate for 15min at 37℃;
[0056] (2) Combine the above reagent series with 25μl magnetic separation reagent of Example 1 and continue incubating at 37°C for 5 minutes;
[0057] (3) Wash 3 times with a cleaning solution to remove unbound antibodies and impurities;
[0058] (4) Add 150μl of the luminescent substrate solution of Example 1, and use Leadman's self-developed chemiluminescence detector to measure the relative luminescence intensity (RLU) after ALP catalyzes the luminescence of the substrate. The results are shown in Table 1 below:
[0059] Table 1
[0060] Calibrator (mg / dL)01.53.572060...
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