Kit for measuring lipoprotein phospholipase A2 and preparation method of kit
A technology for phospholipase and lipoprotein, which is applied in the field of a kit for determining lipoprotein phospholipase A2 and the field of preparation thereof, can solve the problems of low measurement accuracy, complicated operation and the like, and achieves high sensitivity, no radioactive pollution, and improved measurement accuracy. Effect
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Embodiment 1
[0065] The kit of the present invention includes reagent R1 and reagent R2 two-liquid components independent of each other, wherein
[0066]Reagent R1:
[0067] MES buffer 100mmol / L
[0068] Potassium chloride 300 mmol / L
[0069] Polyethylene glycol-2000 10 g / L
[0070] EDTA·2Na 25 mmol / L
[0071] Sodium sorbate 0.6 g / L
[0072] The solvent is purified water
[0073] Reagent R2:
[0074] MES buffer 100 mmol / L
[0075] Bovine Serum Albumin 11 g / L
[0077] Latex coated anti-lipoprotein phospholipase A2 antibody 5 g / L
[0078] Its solvent is purified water.
Embodiment 2
[0080] The kit of the present invention includes reagent R1 and reagent R2 two-liquid components independent of each other, wherein
[0081] Reagent R1:
[0082] Tris buffer 20 mmol / L
[0083] Potassium sulfate 200 mmol / L
[0084] Polyvinylpyrrolidone 25 g / L
[0085] Diethyltriaminepentaacetic acid 45 mmol / L
[0086] Sodium sorbate 0.2 g / L
[0087] The solvent is purified water
[0088] Reagent R2:
[0089] Tris buffer 150 mmol / L
[0090] Bovine serum albumin 18 g / L
[0091] Sodium sorbate 0. 9 g / L
[0092] Latex coated anti-lipoprotein phospholipase A2 antibody 1 g / L
[0093] Its solvent is purified water.
Embodiment 3
[0095] Kit preparation and method of use
[0096] 1. Preparation of latex-coated anti-lipoprotein phospholipase A2 antibody: first dilute polystyrene microspheres with a particle size of 120 nm with 50 mmol / L MES buffer to obtain a mass concentration of polystyrene microspheres of 5% solution, and then add 1.0 mg of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride in every milliliter of solution, react for 1 hour under the condition of 26 ℃, then Use a centrifuge to centrifuge at a speed of 25000 rpm / min for 30 minutes, remove the supernatant, dilute the precipitate with 50 mmol / L MES buffer, then use an ultrasonic disperser for ultrasonic dispersion, and then use a centrifuge to disperse at 25000 rpm Centrifuge for 30 minutes at a speed of 1 / min, remove the supernatant, and then dilute the precipitate with 50 mmol / L MES buffer until the mass concentration of polystyrene microspheres is 4%, use an ultrasonic disperser to disperse, and then Add anti-lipoprotein pho...
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Abstract
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