Lateral antibody chip for detecting three mycotoxins by using marker-guided universal probe
A mycotoxin and antibody chip technology, used in biological testing, measuring devices, material inspection products, etc., can solve probe mutual interference, misjudgment, orderly release of immune chip signal probes, specific identification and complex background control, etc. It can improve the detection signal intensity and sensitivity, improve the detection sensitivity and quantitative precision, and achieve the effect of good hydrophilicity.
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Embodiment 1
[0046] A label-guided universal probe for detecting three kinds of mycotoxins lateral antibody chip, including a liner 5, and bifunctional antigen release pads 1 that are sequentially adhered to the liner 5 and partially overlapped between adjacent ones, universal Fluorescent probe release pad 2, cellulose acetate membrane 3, and water-absorbing pad 4; the bifunctional antigen release pad contains a detection antigen formed by coupling ovalbumin with AFB1, OTA, and ZEN, respectively. - Amino-4-hydroxyl-2-naphthalenesulfonic acid" label 62; the universal fluorescent probe release pad comprises a universal fluorescent probe labeled with an anti-7-amino-4-hydroxyl-2-naphthalenesulfonic acid antibody 65 Needle, 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 C respectively immobilize anti-AFB1 antibody...
Embodiment 2
[0056] Assay method for simultaneous detection of AFB1, OTA, and ZEN, see 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 AFB1, OTA and ZEN.
[0058] refer to Figure 5 . The AFB1 antibody 311 immobilized on the nitrocellulose membrane detection line A, and the anti-7-a...
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