Lipoprotein (a) determination kit and preparation method thereof
A lipoprotein and kit technology, applied in the fields of medicine and biochemistry, can solve problems such as radioactive pollution, low measurement accuracy, complicated operation, etc., and achieve good protection, accurate results, and good stability
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Embodiment 1
[0073] The kit of the present invention includes reagent R1 and reagent R2 two-liquid components independent of each other, wherein
[0074] Reagent R1:
[0075] MES buffer 100mmol / L
[0076] Bovine Serum Albumin 13 g / L
[0077] Polyethylene glycol-8000 30g / L
[0078] Sodium Benzoate 0.9 g / L
[0079] Rabbit anti-human monoclonal antibody 1.0g / L
[0080] The solvent is purified water
[0081] Reagent R2:
[0082] MES buffer 80mmol / L
[0083] Tween-80 1.5 mL / L
[0084] Bovine serum albumin 20 g / L
[0085] Sodium alginate 17g / L
[0086] Sodium Benzoate 0.9 g / L
[0087] Latex-coated anti-human lipoprotein (a) antibody 1g / L
[0088] Its solvent is purified water.
Embodiment 2
[0090] The kit of the present invention includes reagent R1 and reagent R2 two-liquid components independent of each other, wherein
[0091] Reagent R1:
[0092] HEPES buffer 185 mmol / L
[0093] Trehalose 18 g / L
[0094] Polyethylene glycol-6000 20 g / L
[0095] Phenol 0.5 g / L
[0096] Goat anti-human polyclonal antibody 0.2g / L
[0097] The solvent is purified water
[0098] Reagent R2:
[0099] HEPES buffer 50 mmol / L
[0100] Tween-80 0.5 mL / L
[0101] Trehalose 14 g / L
[0102] Gum Arabic 25 g / L
[0103] Phenol 0.5g / L
[0104] Latex-coated anti-human lipoprotein (a) antibody 2g / L
[0105] Its solvent is purified water.
Embodiment 3
[0107] Kit preparation and method of use
[0108] 1. Preparation of latex-coated anti-human lipoprotein (a) antibody: Dilute polystyrene microspheres with a particle diameter of 120 nm to a mass concentration of polystyrene microspheres contained in 50 mmol / L MES buffer solution. 3% solution, and then add 0.5 mg 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride to each milliliter solution, react at 26°C for 2 hours, use centrifugation machine, centrifuge at 15000 rpm / min for 30 minutes, remove the supernatant, suspend the precipitate in 50 mmol / L MES buffer solution, use an ultrasonic disperser for ultrasonic dispersion, and then use a centrifuge at 15000 rpm / min Centrifuge for 30 minutes at a high speed, remove the supernatant, suspend the pellet in 50 mmol / L MES buffer, ultrasonically disperse, then add an equal volume of MES buffer containing anti-human lipoprotein (a) antibody while stirring, Mix and stir, and react for 2 hours at room temperature at 25°C, so t...
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