Kit and method for fast separating virus nucleic acid from biological sample
A virus nucleic acid and kit technology, applied in the field of nucleic acid separation, can solve the problems of poor versatility, expensive viral nucleic acid extraction kits, etc.
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[0043] Embodiment 1: the extraction of HEVRNA
[0044] Serum samples containing HEV were taken for 10-fold serial dilution, and then HEV RNA was extracted with this kit, and Chemagen’s viral nucleic acid extraction kit was used as a control. Follow the steps below to extract HEV RNA:
[0045] (1) Take 100 μl of the serially diluted HEV-containing serum sample and put it in a centrifuge tube, add 5ul (20μg / μl) ProteinaseK and 100μl of lysis buffer, mix well, and place at 55°C for 10 minutes.
[0046] (2) Add 20 μl of magnetic bead suspension (shake well before use) to the above mixture, mix thoroughly, and mix gently and thoroughly at room temperature for 10 minutes.
[0047] (3) Place the centrifuge tube on a magnetic stand, magnetically separate for 30 seconds, and discard the supernatant.
[0048] (4) Add 250 μl of washing buffer I, oscillate to fully suspend the magnetic beads, separate with a magnetic stand after 1 minute, and discard the supernatant.
[0049] (5) Add 2...
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