Method for extracting DNA from formalin-fixed tissue
A formalin and tissue technology, applied in the field of DNA extraction from tissue, can solve the problems of DNA separation failure, inhibition of PCR reaction, expensive Triton-100, etc.
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[0023] The method for extracting DNA from formalin-fixed tissue provided by the invention comprises the following steps:
[0024] 1. Cut out about 30mg of fixed tissue and put it into a 1.5ml EP centrifuge tube;
[0025] 2. Shred as much as possible so that the tissue cells can be completely lysed and digested in step 6;
[0026] 3. Rinse the tissue fragments with graded ethanol (30%, 40%, 50%, 60%, 70%, 80%, 90% and 100%) for 20 minutes each time, and centrifuge at 3000g for 10 minutes to gradually remove Fu Marlin;
[0027] 4. Put it in a silica gel desiccator and let it stand overnight to completely remove formalin;
[0028] 5. Add 300 μl of cell lysate (500 mmol / L Tris pH8.0, 20 mmol / L EDTA, 10 mmol / L NaCl, 1% SDS) and 20 μl of proteinase K (20 mg / ml);
[0029] 6. Shake and mix for 1 minute, then place at 55°C for 2 days to digest the protein, and shake 2-3 times during the process to promote digestion;
[0030] 7. Take out the sample, mix gently after cooling down to ...
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