Application of polyethyleneimine compound in luminescence method in-vitro diagnostic reagent
A technology of polyethyleneimine and in vitro diagnosis, which is applied in chemiluminescence/bioluminescence, analysis and measurement devices through chemical reactions of materials, and can solve the sensitivity and low precision interference of kits and uneven distribution of particles Polymerization, high background and other problems, to achieve the effect of expanding the coating surface area, speeding up the reaction speed, and improving the sensitivity
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Embodiment 1
[0034] Take 15ml of magnetic particles with a particle size of 2 μm, wash and resuspend, add 60ul of EDC and NHS each, mix well and incubate for 20min to obtain activated magnetic particles. Add 15 mg of cTnI monoclonal antibody I to be cross-linked to the activated magnetic particles, and incubate for 3 h with MES buffer (100 mM) as the reaction medium. The supernatant was removed by magnetic adsorption, and the product was resuspended by adding a Tris solution containing 0.07% PEG-g-PEI and 0.9% NaCl, and blocked by shaking for 7 hours. Afterwards, magnetic separation and ultrasound were used to wash the magnetic microspheres coupled with the antibody, and diluent was used to dilute to a concentration of 10 mg / ml to preserve R1. The diluent is PBS 20mM, 0.5% BSA, 0.2% TW-20, 0.9% NaCl, 5% trehalose, 0.1% NaN 3 , pH=7.1. The sensitivity of the diagnostic reagent prepared by this embodiment reaches 0.9 pg / ml when used.
Embodiment 2
[0036] Compared with Example 1, the difference is that PEG-g-PEI is 0.01% PEG-g-PEI. The sensitivity of the diagnostic reagent prepared by this embodiment reaches 1.4 pg / ml when used.
Embodiment 3
[0038] Compared with Example 1, the difference is that PEG-g-PEI is 0.2% PEG-g-PEI. The sensitivity of the diagnostic reagent prepared by this embodiment reaches 1.8 pg / ml when used.
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