Enzyme catalysis conductance immune sensor and method for detecting food-borne causal agent
An immunosensor, food-derived technology, applied in the field of biological analysis, can solve the problems of low specificity, low sensitivity, cumbersome and time-consuming operation, etc., and achieve the effect of simple detection steps, high sensitivity, and simple preparation
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Embodiment 1
[0029] Example 1: Detection of Salmonella by an immunosensor based on microgap array electrodes.
[0030] 1. Preparation of immunosensor:
[0031] The micro-gap array gold electrode produced by the conventional photolithography printing method is used as the substrate, which is an interdigitated double electrode, and the positive and negative electrodes are two comb-shaped gold electrodes, which cross each other to form a micro-gap array gold electrode. Comb tooth width is 1μm-100μm, gap is 1μm-100μm;
[0032] After washing the microgap array gold electrode with absolute ethanol (100%) three times (1 min each time), the electrode was immersed in 1M NaOH solution for 30 min; then the electrode was washed with ultrapure water three times (1 min each time), and dried; Then, the electrode is immersed in an ethanol solution containing 5% (volume percentage) of aminopropyltrimethoxysilane, and left to stand at room temperature for 24 hours; it is washed with ultrapure water three t...
Embodiment 2
[0037] Example 2: Detection of Escherichia coli O157:H7 by an immunosensor based on micro-gap array electrodes.
[0038] 1. Preparation of immunosensor:
[0039]The micro-gap array gold electrode produced by the conventional photolithography printing method is used as the substrate, which is an interdigitated double electrode, and the positive and negative electrodes are two comb-shaped gold electrodes, which cross each other to form a micro-gap array gold electrode. Comb tooth width is 1μm-100μm, gap is 1μm-100μm;
[0040] After washing the microgap array gold electrode with absolute ethanol (100%) three times (1 min each time), the electrode was immersed in 1M NaOH solution for 30 min. Then wash the electrode three times with ultrapure water (each time for 1 min), and dry it. Then, the electrode is immersed in an ethanol solution containing 5% (volume percentage) of aminopropyltrimethoxysilane, and left to stand at room temperature for 24 hours; it is washed with ultrapure...
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