Sarafloxacin immune colloidal gold detection card and preparation method thereof
A technology of colloidal gold and detection cards, which is applied to measuring devices, instruments, scientific instruments, etc., to achieve accurate results and simple methods
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Embodiment 1
[0021] figure 1 , figure 2 Shown embodiment: among the figure 9 is a PVC rubber sheet; 7 is a sample pad; 8 is a colloidal gold binding pad, and the colloidal gold binding pad is coated with a monoclonal antibody colloidal gold marker; 10 is a coating film, i.e. nitrocellulose Plain membrane, the nitrocellulose membrane is coated with sarafloxacin-BSA and goat anti-mouse IgG; 11 is a water-absorbing pad, made of water-absorbing materials such as filter paper.
[0022] On one end (sample end) of the PVC rubber plate 9, the sample pad 7 and the bonding pad 8 are adhered, and the sample pad 7 and the bonding pad 8 are in a side-by-side structure.
[0023] A nitrocellulose membrane 10 is adhered in the middle of the PVC rubber sheet 9 . Goat anti-mouse IgG quality control line 3 and sarafloxacin-BSA detection line 2 are set on the nitrocellulose membrane 10 .
[0024] At the other end of the PVC rubber sheet 9, a water-absorbing pad 11 is adhered. One end of the nitrocellulos...
Embodiment 2
[0026] The preparation of the sarafloxacin colloidal gold detection card is specifically realized by the following steps:
[0027] Preparation of colloidal gold solution: Take a 1 L Erlenmeyer flask, add 495 mL of ultrapure water, and then add 1% chloroauric acid (HAuCl 4 ·3H 2 (0) 5 mL, prepared into 500 mL 0.01% chloroauric acid aqueous solution, heated and boiled, then added 1% trisodium citrate (Na 3 C 6 h 5 o 7 2H 2 O) Solution 5-7 mL, continue to stir and heat, when the color of the solution turns completely transparent purple red, stop heating after maintaining for 5 min, add water to the original volume, cool to room temperature, and store at 2-8°C for later use;
[0028] Antibody pretreatment: centrifuge the sarafloxacin antibody to be labeled at 1000 r / min, 4°C for 20 min, take the supernatant, and dilute it to 1 mg / mL with 0.01 mol / L PBS; or use 0.01 mol / L Dilute to 1 mg / ml in PBS, pass through a 0.22 µm filter membrane;
[0029] Preparation of colloidal gold...
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