A liquid-phase chip and method for simultaneously detecting antibodies to five poultry vertically transmitted diseases
A liquid phase chip and vertical transmission technology, applied in the field of immunochemistry, can solve the problems of high cost, long detection time, weak batch detection ability, etc., and achieve the effect of improving efficiency, high sensitivity, and shortening the detection cycle
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Embodiment 1
[0058] Example 1: A preparation method of coupled magnetic beads in a liquid chip for simultaneous detection of five poultry vertically transmitted diseases
[0059] In the screening process of a large number of studies in the early stage of the present invention, it was found that only the antigenic protein avian influenza virus NP protein, avian Newcastle disease virus NP protein, avian reovirus δC protein, avian leukosis virus P27 protein, avian reticuloendotheliosis virus The env protein is used in the preparation of the liquid phase chip at the same time, so as to realize the accurate infection of five viruses, namely, avian influenza virus, avian Newcastle disease virus, avian reovirus, avian leukosis virus, and avian reticuloendotheliosis virus. , High sensitivity, rapid, high throughput detection.
[0060] The liquid phase chip is prepared as the above five antigen proteins (avian influenza virus NP protein, avian Newcastle disease virus NP protein, avian reovirus δC p...
Embodiment 2
[0068] Example 2: A preparation method of coupled magnetic beads in a liquid chip for simultaneous detection of five poultry vertically transmitted diseases
[0069] 1) Pretreatment of magnetic beads: Take 5 kinds of blank magnetic beads with different codes, centrifuge them at 10000g for 3min, discard the supernatant, resuspend the blank magnetic beads with activation buffer, vortex for 30s, ultrasonically disperse for 60s, and centrifuge at 12000g 2min and discard the supernatant, repeat 3 times; the activation buffer is 0.1M phosphate buffer saline (PBS), its pH is 6;
[0070] 2) Activation of magnetic beads: Resuspend the magnetic beads after the five pretreatments in the previous step in PBS, vortex for 60 s, and ultrasonically disperse for 60 s, then add 10 μl and 50 mg / mL of nitrogen hydroxysuccinimide sulfonate in sequence Sulfo-NHS and 10 μl, 50 mg / mL carbodiimide (EDC), mixed well, and kept in the dark for 20 minutes at 37°C to obtain activated magnetic beads;
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Embodiment 3
[0076] Example 3: A liquid chip for simultaneous detection of five poultry vertically transmitted diseases
[0077] The liquid chip described in this example contains the coupled magnetic beads prepared in Example 1 or 2, a detection antibody and a reporter molecule.
[0078] The detection antibody is a biotin-labeled anti-chicken IgG antibody.
[0079] The reporter molecule is fluorescent protein or fluorescein-labeled streptavidin.
[0080] The fluorescent protein or fluorescein is selected from one of phycoerythrin, Cy3 and Cy5.
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