See all protocols

Gel Extraction using GeneJET Kit

Objective

Author(s): Pattarin Blanchard

Isolate and purify DNA fragments from agarose gel for downstream cloning experiments.

Materials

Procedure

Gel extraction

  1. Weigh and record a microcentrifuge tube for each extraction.
  2. Cut away the desired gel slice using a clean scalpel or razor blade and place into the preweighed tube.
  3. Add 1:1 volume (uL) : weight (mg) ratio of binding buffer (e.g. 100 uL binding buffer for 100 mg gel slice).
  4. Incubate tube at 50-60 C for 10 minutes (until gel is completely dissolved). Invert the tube every few minutes to aid dissolution.
  5. (OPTIONAL) if DNA is:
    1. <500 bp, add the same volume isopropanol as binding buffer in step 3 and mix thoroughly.

    2. 10 kb, add the same volume ultrapure water as binding buffer in step 3 and mix thoroughly.

Gel purification

  1. Transfer up to 800 uL (at a time) of the dissolved gel to a purification column.
  2. Centrifuge at 12,000 g or rcf (not rpm) for 1 minute. Discard flow-through and reuse collection tube.
    1. See additional step if preparing DNA for sequencing in the linked manual.
  3. Add 700 uL wash buffer supplemented with ethanol (should have been done on the first use) to the purification column.
  4. Centrifuge at 12,000 g or rcf for 1 minute. Discard flow-through and reuse collection tube.
  5. Centrifuge again at 12,000 g or rcf for 1 minute to remove residual wash buffer.
  6. Place purification column into a new microcentrifuge tube.
  7. Add 30-50 uL elution buffer or ultrapure to the centre of the column membrane. Centrifuge at 12,000 g or rcf for 1 minute and discard the column.
    1. 50 uL is the standard volume, however if DNA weight is expected to be low, reduce down to 30 uL.
  8. Nanodrop to determine concentration. See NanoDrop Spectrophotometer. Remember to blank with UPH2O.