PCR purification
From 2007.igem.org
Using QIAquick kit
Add 5 volumes of Buffer PBI to 1 volume of sample.
Pipette into a QIAquick spin column(max 770 µl) and centrifuge for 60 sec at 10,000g
Discard flow-through.
Wash: add 0.75ml Buffer PE(make sure that the buffer has ethanol added to it) to column and centrifuge for 1 min
Discard flow-through & centrifuge for 1 min
Place column into clean Eppendorf tube
Add 50ul Buffer EB or water to center of membrane
Let stand at RT for 3 min
Centrifuge for 5 min.
Measure the concentration using the UV spectrophotometer.