Method for direct extraction of nucleic acid without tissue grinding
An extraction method and nucleic acid extraction technology, which are applied in the fields of biochemical equipment and methods, recombinant DNA technology, and the determination/inspection of microorganisms to achieve the effects of fast extraction, stable results and easy operation.
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[0039] 1. Mouse liver DNA extraction
[0040] Manual reagent addition steps (if it is a sealed kit, add 125 μl lysate TR to each well of the first 96 deep-well plate, add 20-60 mg of mouse liver, 20 μl proteinase K, 4 μl RNase, and then directly on the computer):
[0041] 1) Add 250 μl magnetic bead binding solution CB, 125 μl lysis solution TL and 125 μl lysis solution TR, 20 μl proteinase K, 4 μl RNase and about 10 mg tissue sample to the first 96 deep-well plate;
[0042] 2) Add 300 μl buffer BB and 20 μl magnetic beads to each well of the second deep well plate;
[0043] 3) Add 900 μl inhibitor remover IR to each well of the third and fourth deep well plates;
[0044] 4) Add 900 μl of washing solution WB to each well of the fifth deep well plate;
[0045] 5) Add 150 μl of elution buffer TE to each well of the sixth deep well plate;
[0046] 6) Place the deep-well plates in the positioning seats of the 96 nucleic acid extractor in sequence, and then insert the stirring ...
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