Rapid detection method, liquid chip and kit for four human infectious diseases
A liquid phase chip and infectious disease technology, which is applied in the fields of life science and biology, can solve the problems of decreased activity of cells and viruses, low degree of detection reaction, and inconspicuous color results, etc., to achieve high activity and increase the effect of detection
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Embodiment 1
[0023] Example 1: 100 parts of sample diluent, 20 parts of oligonucleotide for HIV detection, 10 parts of HIV positive control, 0.1 part of insulin, 50 parts of amino acid, 0.5 part of DNA polymerase, 0.5 part of reverse transcriptase, RNA polymerase Mix 0.5 parts of enzyme, 10 parts of nucleic acid release agent, 5 parts of targeted nucleotide detection primers, 5 parts of TP positive control, 10 parts of anti-hepatitis B pre-S1 antigen monoclonal antibody and 5 parts of PCR amplification reaction reagent to prepare the solution Phase chip, sealed by the kit, then extract 100ml serum sample and add Trizol, let stand at room temperature for 5min, centrifuge at 1000g centrifuge for 10min at 10°C, extract the supernatant to another reagent tube, and centrifuge again at 10°C Centrifuge at 1000g for 10min, remove the supernatant, take out the centrifuged serum for later use, drop 25ml of centrifuged serum into the kit at room temperature, shake well and let it stand for 5min at 25°...
Embodiment 2
[0024] Example 2: 100 parts of sample diluent, 10 parts of oligonucleotides for HIV detection, 5 parts of HIV positive controls, 0.2 parts of insulin, 50 parts of amino acids, 0.5 parts of DNA polymerase, 0.5 parts of reverse transcriptase, RNA polymerase Mix 0.5 parts of enzyme, 20 parts of nucleic acid release agent, 10 parts of targeted nucleotide detection primers, 5 parts of TP positive control, 10 parts of anti-hepatitis B pre-S1 antigen monoclonal antibody and 5 parts of PCR amplification reaction reagent to prepare the solution Phase chip, sealed by the kit, then extract 100ml serum sample and add Trizol, let stand at room temperature for 5min, centrifuge at 1000g centrifuge for 10min at 10°C, extract the supernatant to another reagent tube, and centrifuge again at 10°C Centrifuge at 1000g for 10min, remove the supernatant, take out the centrifuged serum for later use, drop 25ml of centrifuged serum into the kit at room temperature, shake well and let it stand for 5min ...
Embodiment 3
[0025]Example 3: 100 parts of sample diluent, 10 parts of oligonucleotides for HIV detection, 5 parts of HIV positive controls, 0.1 parts of insulin, 20 parts of amino acids, 0.2 parts of DNA polymerase, 0.2 parts of reverse transcriptase, RNA polymerase Mix 0.2 parts of enzyme, 10 parts of nucleic acid release agent, 5 parts of targeted nucleotide detection primers, 5 parts of TP positive control, 20 parts of anti-hepatitis B pre-S1 antigen monoclonal antibody and 5 parts of PCR amplification reaction reagent to prepare the solution Phase chip, sealed by the kit, then extract 100ml serum sample and add Trizol, let stand at room temperature for 5min, centrifuge at 1000g centrifuge for 10min at 10°C, extract the supernatant to another reagent tube, and centrifuge again at 10°C Centrifuge at 1000g for 10min, remove the supernatant, take out the centrifuged serum for later use, drop 25ml of centrifuged serum into the kit at room temperature, shake well and let it stand for 5min at...
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