Method for preparing acetylcholinesterase fluorescence biosensor
An acetylcholinesterase and biosensor technology is applied in the field of preparation of acetylcholinesterase fluorescent biosensors, which can solve the problems of inability to use the biosensor multiple times, high instrument cost, loss of enzymatic activity, etc., and achieves continuous and controllable operation and low cost. Inexpensive and simple process
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specific Embodiment approach 1
[0007] Specific embodiment 1: In this specific embodiment, 1. A preparation method of acetylcholinesterase fluorescent biosensor, characterized in that the steps of the preparation method of acetylcholinesterase fluorescent biosensor are as follows: 1. Acetylcholinesterase extraction: 1 , Store the purchased live crucian carp head in a self-made ice box, cut the skull, and then take out the entire brain tissue with tweezers, remove blood streaks with filter paper, and remove non-brain tissue, and place it in a watch glass for weighing. 2. Tris-HCl extraction method Homogenize under the condition of Tris-HCl ice bath containing 0.1% Triton X-100 and 0.05mol / L NaCl (every 15s, 5s interval). The homogenate was centrifuged (10000r / min) at 0~4℃ for 10min. 2. Purification: 1. Desalting. After ammonium sulfate fractionation and salting out, the enzyme solution dissolved in Tris-Hcl (0.07mol / l, pH=8) is put into a dialysis bag, and the distilled water is dialyzed for 48h, and BaCl is used...
specific Embodiment approach 2
[0008] Specific embodiment two: this specific embodiment is different from specific embodiment one in that it is characterized in that in step one, the extraction of acetylcholinesterase adopts pH=8.0~10.0Tris-HCl solution and homogenize 4~4 under ice bath conditions. 10min (every 15s, intermittent 5s), the homogenization ratio (mass:volume) is 1:5. Others are the same as the first embodiment.
specific Embodiment approach 3
[0009] Specific embodiment three: this specific embodiment is different from specific embodiment one in that it is characterized in that step two is purified by Sephadex G-200 gel chromatography column, and the eluent is 0.1-0.2 mol / L phosphate buffer , The flow rate is 0.15mL / min. Others are the same as the first embodiment.
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