Flunixin meglumine monoclonal antibody hybridoma cell strain YY and application thereof
A technology of flunixin meglumine and hybridoma cell lines, applied in biochemical equipment and methods, material inspection products, instruments, etc., can solve problems such as low sensitivity, difficulty in obtaining accurate results, lengthy separation and purification process, etc., and achieve The effect of good specificity and good detection sensitivity
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[0018] Embodiment 1 Preparation of hybridoma cell line YY
[0019] (1) Preparation of complete antigen: Weigh 2.2 mg FM, 2.6 mg 1-ethylcarbodiimide hydrochloride, 1.6 mg N-hydroxysuccinimide, and dissolve with 400 μL anhydrous N,N-dimethylformaldehyde The amide was dissolved and stirred at room temperature for 6-8h (referred to as solution A). Take 10 mg of bovine serum albumin BSA (the molar ratio of FM to BSA is 30:1), and dissolve it with 4 mL of boric acid buffer solution (called solution B). At room temperature, add solution A to solution B dropwise, and react overnight at room temperature to obtain the conjugate FM-BSA mixture, and separate the complete antigen and unconjugated small molecule hapten by dialysis. Preparation of coated original FM-OVA: Weigh 1.6mg FM, 1.9mg 1-ethylcarbodiimide hydrochloride, 1.2mg N-hydroxysuccinimide, add 300μL anhydrous N,N-dimethyl Dissolve the formamide and stir at room temperature for 6-8 hours (referred to as liquid A). Weigh 5 mg...
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