Mycotoxin magnetochemiluminescence immunoassay kit based on bifunctional fusion protein and application of mycotoxin magnetochemiluminescence immunoassay kit
A mycotoxin and fusion protein technology, applied in enzyme fusion, analytical materials, immunoglobulin, etc., can solve problems such as low coupling efficiency, reduced sensitivity, and heterogeneous conjugates, and achieve simple expression, stable process, and process flow long effect
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Embodiment 1
[0044] Example 1 Preparation of aflatoxin B1 nanobody-alkaline phosphatase bifunctional fusion protein
[0045] AFB1-scFV-AP bifunctional fusion protein is obtained by using alkaline phosphatase as a bioluminescent catalyst, and the aflatoxin B1 nanobody (AFB1 scFv) is fused and expressed with alkaline phosphatase (AP).
[0046] AFB1-scFV-AP bifunctional fusion protein was prepared by the following method:
[0047] (1) Design and synthesis of AFB1 Nanobody gene: According to the amino acid sequence SEQ ID NO:7 of AFB1 Nanobody, the efficient expression of the gene in E. coli was achieved by optimizing the structure of the gene, including the use of E. coli preferred codons to eliminate possible The secondary structure of the GC / AT was balanced, etc., and the nucleotide fragment of the AFB1 Nanobody gene was designed and synthesized (the nucleotide sequence is shown in SEQ ID NO: 8).
[0048] (2) Construction of AFB1-scFV-AP expression vector: The aflatoxin B1 nanobody gene sy...
Embodiment 2
[0055] Example 2 Preparation of deoxynivalenol enol nanobody-alkaline phosphatase bifunctional fusion protein
[0056] Using the method of Example 1, a DON-scFV-AP bifunctional fusion protein was prepared, the amino acid sequence of which is shown in SED ID NO:2.
Embodiment 3
[0057] Example 3 Preparation of Zearalenone Nanobody-Alkaline Phosphatase Bifunctional Fusion Protein
[0058] Using the method of Example 1, a ZEN-scFV-AP bifunctional fusion protein was prepared, the amino acid sequence of which is shown in SED ID NO:3.
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