PCR Purification

Goal

The aim of the PCRpurification step is to recover DNA from PCR and other enzymatic reacti mixtures.

Preparation

1.
Add 1:1 volume of Binding Buffer to completed PCR mixture (e.g. if you have 100 µL of reaction mixture, add 100 µL of Binding Buffer). Mix thoroughly and check the solution's color: a yellow color color indicates an optimal pH for DNA binding.
If the color of the solution is orange or violet, add 10 µL of 3 M sodium acetate, pH 5,2 and mix. The color will become yellow.
If the DNA fragment is superior to 500 bp, add a 1:2 volume of 100% isopropanol (e.g. if you have 100 µL of PCR mixture combined with 100 µL (total amount of 200 µL), add 100 µL isopropanol). Mix thoroughly.

2.
Transfer up 800 µL of the solution from step previous step to the GeneJET purification column.
Centrifuge for 30-60 seconds, then discard the flow-through.

3.
Add 700 µL of Wash Buffer (previously dilted with ethanol) to the purification column.
Centrifuge for 30-60 seconds, then discard the flow-through and place the purification column back into the collection tube?

4.
Centrifuge the empty GeneJET purification for 1 minute to completely remove any residual wash buffer

5.
Transfer the GeneJET purification column to a clean 1,5 mL tube.
Add 50 µL of Elution Buffer to the center of the GeneJET purification column membrane and centrifuge for 1 minute.

6.
Discard the GeneJET purification column and store the purified DNA at -20°C.

7.

8.

Test