Pathogenic bacteria immune detection chip and preparation method thereof
An immunological detection and pathogenic technology, applied in measuring devices, instruments, scientific instruments, etc., can solve the problems of time-consuming and labor-intensive, false positives, etc., and achieve the effect of reliable results and time-saving and labor-saving results.
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[0010] Example 1
[0011] 1. Glass slide treatment
[0012] 1). Slide cleaning
[0013] Take the slides, wash them with water, put them in a solution composed of 1 / 3 hydrogen peroxide and 2 / 3 concentrated sulfuric acid, and soak them for 0.5-3.0 hours. Then rinse with deionized water or distilled water for 2-6 times, then boil with deionized water or distilled water for 2-30 minutes; dry under nitrogen flow, and store in a dry place for future use.
[0014] (1) Aminosilanization on the surface of the glass slide The cleaned glass slide was immersed in a solution of 95% acetone / water containing 0.1-10.0% aminopropyltriethoxysilane for 3-30 minutes, and then taken out After that, the slides were washed 2-6 times with acetone for 1-5 minutes each time, and then washed with deionized distilled water for 1-5 times for 1-5 minutes each time, and finally dried at 60-180°C and left to dry. save at.
[0015] (2). Aldehyde group modification on the surface of glass slide
[0016] P...
Example Embodiment
[0025] Example 2
[0026] The product of the present invention is a pathogenic bacteria immunodetection chip, comprising: a carrier 1, on which different bacterial antibodies 2 are immobilized by chemical groups containing amino or aldehyde groups arranged on the carrier, and the same The bacterial antibodies are arrayed on the carrier.
Example Embodiment
[0027] Example 3
[0028] The method of the invention is a preparation method for manufacturing a pathogenic bacteria immunodetection chip. First, a glass slide is taken and cleaned, and then the cleaned glass slide is immersed in 0.1-10.0% aminopropyltrimethoxy The solution of 95% acetone / water of base silane for 3-30 minutes, after taking out, the slides were washed 2-6 times with acetone, 1-5 minutes each time, and then rinsed with deionized distilled water 1-5 times, 1 time each time -5 minutes, then dried at 60-180 °C to silanize the surface of the glass slide, then, modify the amino group or aldehyde group on the surface of the glass slide, and finally, set the pathogenic bacterial antibody on the glass slide according to the array. On the slide, put it in a humid environment of 0℃-55℃ for 0.1-72 hours, take it out, wash it 1-5 times with buffer solution with pH 4.0-10, ion concentration 0.00-0.75m / L, the above glass slides The cleaning of the tablet is to clean it with...
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