Homogeneous immunometric fluorescent compound set for quickly and quantificationally detecting heart fatty acid binding-proteins (FABP) and preparation method of homogeneous immunometric fluorescent compound set
A fatty acid binding and immunological reagent technology, applied in the field of medical testing, can solve the problems of non-excitation, low fluorescence value, low non-specific fluorescence, etc., and achieve the effects of low cost, good specificity and simple operation
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Embodiment 1
[0042] 1. Preparation of anti-FABP for labeling:
[0043] Purified monoclonal antibody against cardiac fatty acid binding protein expressed by genetic engineering was selected. Eu 3+ The product code of anti-cardiac fatty acid binding protein monoclonal antibody for labeling is 10E1; the product code of anti-cardiac fatty acid binding protein monoclonal antibody for fluorescein labeling is 9F3 and 5B5.
[0044] 2. Preparation of rare earth element chelate labeled anti-FABP:
[0045] The mouse anti-human H-FABP monoclonal antibody 10E1 solution (3 mg / ml) was dialyzed twice at 4° C. with 3 L of 0.9% NaCl, 24 hr each time. Add water to adjust the concentration to 1.5mg / ml. Take 0.6ml of the antibody solution, add 1ml NaHCO 3 (0.2mol / L), and adjust the pH to 9.1 with 1mol / L NaOH. 20 μl of BHHCT methanol solution (30 μg / ml) was added dropwise to the antibody solution under stirring, and the stirring reaction was continued for 1 hr. After centrifugation (10000rpm, 10min) to re...
Embodiment 2
[0051] The preparation method of the present embodiment is basically the same as that of Example 1, the difference is:
[0052] In step 2, the preparation method of rare earth element chelate-labeled anti-FABP is: dialyze the mouse anti-human H-FABP solution (3 mg / ml) twice at 4° C. with 3 L of 0.9% NaCl, 24 hr each time. Add water to adjust the concentration to 1.5mg / ml. Take 0.6ml of the antibody solution, add 1ml NaHCO 3 (0.2mol / L), and adjust the pH to 9.1 with 1mol / LNaOH. 20 μl of BHHBCB methanol solution (30 μg / ml) was added dropwise to the antibody solution under stirring, and the stirring reaction was continued for 1 hr. After centrifugation (10000rpm, 10min) to remove insoluble matter, put on SephadexG-25 column, use 0.05mol / L NH 4 HCO 3 (pH8.0) to separate the labeled protein and free label. UV / visible spectrophotometer detects the A of each collection liquid 330 value, pool the solutions containing the labeled antibodies. Add final concentrations of 0.1% BSA ...
Embodiment 3
[0054] The preparation method of the present embodiment is basically the same as that of Example 1, the difference is:
[0055] In step 3, the anti-H-FABP monoclonal antibodies 9F3 and 5B5 were diluted to 1mg / ml with 0.1M sodium bicarbonate solution respectively, 5ml of the antibody solution was taken respectively, and 40mg of fluorescein DyLight-DY647 solution was added, and stirred evenly. Incubate at room temperature for 1.5 hours, mixing every 15 minutes. Finally, use a G25 gel column to separate and purify, collect the labeled fluorescein-labeled antibody, dilute it with 0.01M phosphate buffer containing 0.025% PEG, 2.5% BSA, 15% glycerol, and 0.03% surfactant. The bottle is sealed and stored at 4°C.
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