Optimal cystatin C detection kit and preparation method thereof
A technology for detecting kits and cystatin, which is applied in the field of biomedicine, can solve problems such as the inability to guarantee product stability and accuracy, the limitation of professional skills of operators, and complicated operations, so as to achieve stable test results, improve accuracy and resist Interference ability, simple operation effect
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Embodiment 1
[0062] The kit of the present invention is exemplified as a double reagent, wherein:
[0063] Reagent R1
[0064]
[0065] Reagent R2:
[0066]
Embodiment 2
[0068] As a preference, the present invention discloses a preferred cystatin C assay kit, which comprises independent reagents R1 and R2 to form the kit, and the components and corresponding contents included are:
[0069]
[0070]
[0071] Polystyrene microspheres coated with cystatin C antibody and β-cyclodextrin particles, particle size 100nm, concentration 1%.
[0072] Calibrator:
[0073]
[0074] According to the required concentration of the cystatin C reference calibrator, the corresponding cystatin C standard was added to the above buffer respectively to prepare a set of calibrator with different concentrations.
Embodiment 3
[0076] How to use the kit:
[0077] 1. Reagent preparation, the reagent is a liquid double reagent, ready to use after opening the bottle, of which:
[0078] (1), preparation of reagent R1:
[0079] Configuration buffer 1: phosphate buffer 10mmol / L;
[0080] Add bovine serum albumin 10g / L, Tween 20 0.2mmol / L, polyethylene glycol 3.5mmol / L, sodium chloride 0.12mol / L, sodium azide 10mmol / L into buffer 1, stir and mix evenly, The reagent R1 is obtained;
[0081] (2), the preparation of reagent R2:
[0082] Step 1: Dialyze the Cystatin C antibody at 4°C, and then dilute the Cystatin C antibody to 2 mg / ml with phosphate buffer to obtain the Cystatin C antibody dilution; Dilute the polystyrene microspheres with purified water Centrifuge and wash 3 times;
[0083] Step 2: Dilute the polystyrene microspheres washed in Step 1 with phosphate buffer solution to a mass concentration of 1.0%, then add 0.3% β-cyclodextrin, stir and react at room temperature for 30 minutes, and the reac...
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