Nucleic acid extraction kit and nucleic acid extraction method
A nucleic acid extraction reagent and nucleic acid technology, applied in biochemical equipment and methods, microbiological measurement/inspection, DNA preparation, etc., can solve the problems of low purity and concentration of extracted nucleic acid, cumbersome extraction kit steps, poisonous and harmful, etc., to achieve The extraction method is simple, the time cost is shortened, and the effect of saving production and application costs
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Embodiment 1
[0072] In this embodiment, the HeLa cell suspension is used as a sample, and the nucleic acid in the sample is extracted. The nucleic acid extraction process of the present embodiment is as follows:
[0073] (1) Add 200 μL of HeLa cell suspension and 200 μL of chelating resin suspension into a 1.5ml centrifuge tube, mix thoroughly by inversion, place at 95°C for 10 minutes, and vortex and shake the mixed solution several times during the process to ensure the chelation Lysis of cells by synthetic resin and specific adsorption of non-nucleic acid impurities;
[0074] (2) Centrifuge the mixed liquid at a speed of 5000rpm for 2 minutes, and draw the supernatant into another new 1.5ml centrifuge tube;
[0075] (3) Add 50 μL of magnetic nanoparticle solution, 20 μL of proteinase K solution, and 250 μL of buffer solution into the centrifuge tube, mix them upside down, and incubate at room temperature for 5 minutes. full adsorption;
[0076] (4) Place the centrifuge tube on the ma...
Embodiment 2
[0086] In this embodiment, the human umbilical vein endothelial cell suspension is used as a sample, and the nucleic acid in the sample is extracted. The nucleic acid extraction process of the present embodiment is as follows:
[0087] (1) Add 200 μL of human umbilical vein endothelial cell suspension and 200 μL of chelating resin suspension into a 1.5ml centrifuge tube, mix thoroughly by inversion, place at 95°C for 10 minutes, and vortex the mixed solution several times during the process The treatment ensures the lysis of cells by the chelating resin and the specific adsorption of non-nucleic acid impurities;
[0088] (2) Centrifuge the mixed liquid at a speed of 5000rpm for 2 minutes, and draw the supernatant into another new 1.5ml centrifuge tube;
[0089] (3) Add 50 μL of magnetic nanoparticle solution, 20 μL of proteinase K solution, and 250 μL of buffer solution into the centrifuge tube, mix them upside down, and incubate at room temperature for 5 minutes. full adsor...
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