Here is the method:
- Picking out of 1 ose of the bacteria colony from the plate into 200 microliters of Prepman ultra reagent (placed in the sterile tube).
- Incubate the reagent+colony in 100 Celcius degree water-bath for 10 minutes.
- Cool the tube at the room temperature for 2 minutes.
- Centrifuge the tube at 10000 rpm for 2 minutes at 4 Celcius degree.
- Taking out the supernatant and leave the cell in the tube.
- Now you have 200 microliters of DNA template.
- You can transfer 5 microliters for the assay.
It is just as simple as that to get the DNA template, thanks to Applied Biosystem for this helpful kit.
Regards