Neutrophile granulocyte gelatinase related lipid transport protein detection kit and preparation method thereof
A technology for lipocalin and neutrophils, which is applied in biological tests, measuring devices, material inspection products, etc., and can solve the problems of poor anti-interference ability, low degree of automation of enzyme-linked immunosorbent assay, and small linear range of measurement. , to avoid the impact of product quality, avoid poor product stability, and solve the effect of insufficient product stability
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Embodiment 1
[0047] Preliminary Example 1 Screening of NGAL Antibody
[0048] 1. Preparation of MMP-9 affinity chromatography column: Mix protein MMP-9 (purchased from R&D Company) and packed CNBr-Sepharose4B (Pharmacia product) at a ratio of 5-7 mg / mL, shake at 4°C for 20 hours, make it cross-linked. Then wash with 0.1 mol / L pH 8.0 carbonate buffer solution for 3 times, then add an equal amount of 0.1 mol / L ethanolamine-HCl and shake at 4°C for 1 hour to block the remaining activated groups. Finally, wash with 0.01mol / L Tris-HCl (TB), pack the column, and equilibrate. The volume of the column is selected as 10mL.
[0049] 2. Preparation of MMP-9 / NGAL complex affinity chromatography column: protein NGAL (purchased from R&D Company) was prepared into a 2 mg / mL solution, and the NGAL protein solution was passed through the MMP-9 affinity column at a flow rate of 1 mL / min. Chromatographic column, the amount of protein solution is 60mL; then excess NGAL protein is eluted with 0.1mol / L pH8.0 ...
Embodiment 2
[0051] Preparation of latex particles coated with NGAL antibody in preliminary example 2
[0052] The preparation process of latex particles coated with NGAL antibody is as follows:
[0053] ①Preparation of carboxylated polystyrene latex solution: Weigh 1.0g of dry polystyrene latex particles with a particle size of 105nm, add 100mL of 0.12M phosphate buffer (pH7.5) to disperse, add 40mg of 1-ethyl -3-(3-Dimethylaminopropyl)carbodiimide (EDC), then add 20mg of thio-NHS, stir the reaction at room temperature for 0.5 hours, centrifuge to discard the supernatant, and then use 100mL of 0.12M phosphate buffer The carboxylated modified polystyrene latex obtained by liquid dilution, dispersion and precipitation latex;
[0054] ② Preparation of NGAL antibody solution: Dissolve 250 μg of the NGAL antibody screened in Preliminary Example 1 with 0.5 mL of deionized water to obtain an NGAL antibody solution;
[0055] ③ Preparation of latex particles coated with NGAL antibody: Take 100 μ...
Embodiment 3
[0056] Preliminary Example 3 Preparation of latex particles coated with NGAL antibody
[0057] The preparation process of latex particles coated with NGAL antibody is as follows:
[0058] ①Preparation of carboxylated modified polystyrene latex solution: Weigh 1.0g of dry polystyrene latex particles with a particle size of 130nm, add 100mL of 0.12M phosphate buffer (pH7.5) to disperse, add 40mg of 1-ethyl -3-(3-Dimethylaminopropyl)carbodiimide (EDC), then add 20mg of thio-NHS, stir the reaction at room temperature for 0.5 hours, centrifuge to discard the supernatant, and then use 100mL of 0.12M phosphate buffer The carboxylated modified polystyrene latex obtained by liquid dilution, dispersion and precipitation latex;
[0059] ② Preparation of NGAL antibody solution: Dissolve 250 μg of the NGAL antibody screened in Preliminary Example 1 with 0.5 mL of deionized water to obtain an NGAL antibody solution;
[0060]③ Preparation of latex particles coated with NGAL antibody: Take ...
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