Cutting Bands from a Gel

Cutting the Bands

  • Fill appropriate number of 500 µL PCR tubes with 50 µL of 10 mM Tris buffer
  • Carefully slide the gel onto the wetted transilluminator plate (wetting the edges of the gel is helpful)
  • Wearing protective equipment, turn on the transmitted UV switch
  • Using a sterilized scalpel (cleaned with 70% ethanol), cut along the top and bottom edges of the band
  • Snip the left and right edges of the band with sterilized forceps (cleaned with 70% ethanol)
  • Remove the excised band and place in corresponding PCR tube
  • Repeat as necessary
  • Store tubes at 4oC for three to five days to allow DNA to diffuse into the buffer

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