A NMR detection method for foodborne pathogens based on fe3o4 nanomaterials
A technology of food-borne pathogenic bacteria and nanomaterials, which is applied in the direction of analysis using nuclear magnetic resonance
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example 1
[0019] Test food samples for the presence of the harmful pathogenic bacteria Listeria.
[0020] 1. Preparation of immunomagnetic beads: coupling of magnetic beads and monoclonal antibodies. Commercially available carboxylated magnetic beads from Aorun Company, PM3-020 (180nm) were coupled with monoclonal antibodies. The monoclonal antibody adopts the commercial Listeria monoclonal antibody purchased by the biological reagent company, or prepares the monoclonal monoclonal antibody by itself and separates and purifies it. Coupling steps: ① Cleaning: Take 5 mg of carboxylated magnetic beads in a 5 mL centrifuge tube, wash twice with 2 mL of phosphate buffer (PB) 0.02M, pH=6.0, and wash with 2 mL of morpholineethanesulfonic acid (MES) Resuspend at 0.05M, pH=6.0; ②Activation: Sonicate to disperse the magnetic beads, then add 1mg carbodiimide (EDC), 1mg N-hydroxysuccinimide (NHSS) (use 0.05M, pH=6.0 MES Dissolved), activated at 25°C for 2 hours, rotator 15r / min to maintain the sus...
example 2
[0025] Determination of food samples for the presence of the harmful pathogen Escherichia coli O157:H7.
[0026] 1. Preparation of immunomagnetic beads: coupling of magnetic beads and monoclonal antibodies. Commercially available carboxylated magnetic beads from Aorun Company, PM3-020 (180nm) were coupled with monoclonal antibodies. The monoclonal antibody adopts the commercial Escherichia coli O157:H7 monoclonal antibody, or prepares the monoclonal monoclonal antibody by itself and separates and purifies it. Coupling steps: ① Cleaning: Take 5mg of carboxylated magnetic beads in a 5mL centrifuge tube, wash twice with 2mL PB (0.02M, pH=6.0), and resuspend with 2mL MES (0.05M, pH=6.0) after washing; ②Activation: Ultrasonic to disperse the magnetic beads, then add 1mg EDC and 1mg NHSS (dissolved with 0.05M, pH=6.0 MES) respectively, activate at 25°C for 2h, and keep the suspension at 15r / min on the rotator; ③Coupling: Magnetic separation, Aspirate the supernatant, wash once wit...
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