Latex enhanced immunoturbidimetry kit for content of helicobacter pylori antibodies
A Helicobacter pylori, latex-enhanced technology, which is applied to measurement devices, material analysis, instruments and other directions by observing the impact on chemical indicators, can solve the problems of result impact, long time consumption, manual operation, etc.
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Embodiment 1
[0094] Example 1: Preparation of Helicobacter pylori Antibody Kit 1
[0095] 1. Preparation of Reagent R1
[0096] In 50mM HEPES buffer at pH 7.2, add 0.9% NaCl by weight / volume, 5% PEG-8000 by weight / volume, 1% BS by weight / volume, 10mM EDTA, 0.1% sodium azide by volume, stir evenly to be R1 reagent.
[0097] 2. Preparation of R2 Reagent
[0098] Polystyrene latex solution (concentration 10% by weight / volume) (purchased from Merck) 0.5mL with a diameter of 150nm, add 4.5mL of 0.05MMES buffer (pH6.0), and then add 0.5mg / ml of cross-linking agent EDAC (purchased from Merck) was activated for 30 minutes;
[0099] Dilute 0.5 mg of Helicobacter pylori antigen (purchased from Calbioreagents) with 5 mL of 0.05 MMES buffer (pH 6.0), immediately add to the above latex solution, and react at 37 ° C for 3 hours;
[0100] Add 1mL of 0.1M glycine buffer (pH7.0) and stir for 1h to stop the reaction, centrifuge to remove the supernatant;
[0101] Wash 3 times with 33 mL of 50 mM glycin...
Embodiment 2
[0106] Example 2: Preparation of Helicobacter pylori Antibody Kit 2
[0107] 1. Preparation of R1
[0108] The preparation method of reagent R1 is the same as in Example 1.
[0109] 2. Preparation of R2 Reagent
[0110] Polystyrene latex solution (concentration 10% by weight / volume) (purchased from Merck) 0.5mL with a diameter of 150nm, add 4.5mL of 0.05MMES buffer (pH6.0); add 0.5mg / ml of cross-linking agent EDAC (purchased from Merck) was activated for 30 minutes;
[0111] After diluting 0.5 mg of Helicobacter pylori antigen containing 0.2% amino-modified PEG-20000 (purchased from Pierce) with 5 mL of 0.05 MMES buffer (pH 6.0), it was immediately added to the above latex solution and reacted at 37 ° C for 3 hours ;
[0112] Add 1mL of 0.1M glycine buffer (pH7.0) and stir for 1h to stop the reaction, centrifuge to remove the supernatant;
[0113] Wash 3 times with 33 mL of 50 mM glycine buffer (pH 8.0), and harvest the latex particles coated with antigen;
[0114] Use 3...
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