Gel clean-up
Excise DNA fragment/solubilize gel slice
- Note: Minimize UV exposure time to avoid damaging the DNA.
- Take a clean scalpel to excise the DNA fragment from an agarose gel. Remove all excess agarose.
- Determine the weight of the gel slice and transfer it to a clean tube.
- For each 100 mg of agarose gel < 2 % add 200 uL Buffer NTI.
- For gels containing <2 % agarose, double the volume of Buffer NTI.
- Incubate sample for 5-10 min at 50 ℃. Vortex the sample briefly every 2-3 min until the gel slice is completely dissolved!
Bind DNA
- Place a NucleoSpin Gel and PCR Clean-up Column into a Collection Tube (2 ml) and load up to 700 ul sample.
- Centrifuge for 30 s at 11,000 x g. Discard flow-through and place the column back into the collection tube.
- Load remaining sample if necessary and repeat the centrifugation step.
Wash silica membrane
- Add 700 ul Buffer NT3 to the NucleoSpin Gel and PCR Clean-up Column. Centrifuge for 30 s at 11,000 x g. Discard flow-through and place the column back into the collection tube.
- Recommended: Repeat previous washing step to minimize chaotropic salt carry-over and improve A(260)/A(230) values.
Dry silica membrane
- Centrifuge for 1 min at 11,000 x g to remove Buffer NT3 completely. Make sure the spin column does not come in contact with the flow-through while removing it from the centrifuge and the collection tube.
- Note: Residual ethanol from Buffer NT3 might inhibit enzymatic reactions. Total removal of ethanol can be achieved by incubating the columns for 2-5 min at 70 ℃ prior to elution.
Elute DNA
- Place the NucleoSpin Gel and PCR Clean-up Column into a new 1,5 mL microentrifuge tube (not provided). Add 15-30 ul Buffer NE and incubate at room temperature (18-25 ℃) for 1 min at 11,000 x g.
- Note: DNA recovery of larger fragments (>1000 bp) can be increased by multiple elution steps with fresh buffer, heating to 70 ℃ and incubation for 5 min.