Antibody array card for detecting three mycotoxins by using difunctional antigen-guided universal signal
A mycotoxin and dual-function technology, applied in the field of food and drug safety testing, can solve the problems of orderly release of immune chip signal probes, complex specific recognition and background control, misjudgment, probe mutual interference, etc., and achieve active protection Favorable, improve detection sensitivity and quantitative precision, improve detection signal strength and sensitivity
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Embodiment 1
[0046] An antibody array card for the detection of three mycotoxins with a dual-function antigen-guided universal signal, including a liner 5, and a dual-function antigen release pad 1 that is sequentially adhered to the liner 5 and partially overlapped adjacent to each other, and a universal fluorescent light Probe release pad 2, cellulose acetate membrane 3, and water-absorbent pad 4; the bifunctional antigen release pad contains the detection antigen formed by coupling ovalbumin with FB1, DON, and F-2 respectively. 7-amino-4-hydroxyl-2-naphthalenesulfonic acid" label 62; the universal fluorescent probe release pad comprises a universal fluorescent probe labeled with anti-7-amino-4-hydroxyl-2-naphthalenesulfonic acid antibody 65 Probe, the fluorescent probe is a quantum dot 61; the cellulose acetate membrane 3 is provided with detection line A, detection line B, detection line C and quality control line 34, the detection line A, detection line B, detection line Line C immobi...
Embodiment 2
[0056] For the detection method of simultaneously detecting FB1, DON and F-2, refer to Figure 6 ,Proceed as follows:
[0057] Take 5g of crushed cereal crop samples, fully extract the sample in 25mL of 70% methanol-water solution, centrifuge at 5000rpm for 10 minutes, take 2.0mL of the supernatant and add it to 8.0mL of PBS buffer, shake well to become the sample solution; use a dropper Add 3-4 drops of sample solution on the bifunctional antigen release pad. During the movement of the sample solution to the nitrocellulose membrane, the bifunctional antigen and the universal fluorescent probe are released, and successively cross the detection line and the quality control line. According to the detection line A, detection line B, detection line C and the fluorescent signal on the quality control line to determine whether the sample contains FB1, DON and F-2.
[0058] refer to Figure 5 . The FB1 antibody 311 immobilized on the nitrocellulose membrane detection line A, and t...
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