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西亚试剂:Genomic DNA Quickprep for PCR

  1. macerate tissue in Eppendorf tube without butter at RT
  2. add 400 ml extraction buffer
  3. vortex for 4 sec
  4. leave sample at RT until other samples are ready (> 1 h)
  5. spin in microfuge for 1 min
  6. transfer 300 ml of supernatant to different Eppendorf tube (prefilled with 300 ml isopropanole)
  7. mix and leave at RT for 2 min
  8. spin for 5 min
  9. vacuum dry pellet and take up in 100 ml TE
  10. use 1-2.5 ml for PCR

 

Remarks:

DNA is stable for one year at 4°C

 

 

Solutions:

 

Extraction buffer:

200 mM Tris-HCl pH 7.5
250 mM NaCl
 25 mM EDTA
0.5%  SDS