Method for preparing visual gene identification and detection reagent based on G4DNAzyme coloration
A technology for identification and detection of genes, applied in the field of genetic engineering, can solve the problems of unsuitability for mass detection, poor specificity and sensitivity, difficulty in identification and detection of swine fever, etc., and achieves the effects of low detection cost, intuitive results, and fast detection speed.
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[0043] Based on G 4 A method for preparing a visual gene identification detection reagent for DNase color development, characterized in that it comprises the following steps:
[0044] A. Extraction of target genes
[0045] Select the cells infected with classical swine fever virus, freeze and thaw three times at -70°C, each time for 10-30 minutes, take 200 μl and add 1ml RNA lysate (Trizol) to mix, let stand at room temperature for 10-15 minutes, add 0.2 ml chloroform, let stand at room temperature for 3-5 minutes, centrifuge at 12000g / min at 4°C for 10-15 minutes, transfer the supernatant to another centrifuge tube, add 0.5ml isopropanol, precipitate at room temperature for 10-20 minutes, and then Centrifuge at 12000g / min at 4°C for 10 minutes, pour off the supernatant, add 1ml of 75% ethanol and centrifuge at 7500g / min at 4°C for 5 minutes, discard the supernatant, dry the RNA pellet at room temperature, add DEPC-treated water 20μl to get target gene RNA;
[0046] The 75%...
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Abstract
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