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From 2010.igem.org

PCR Purification

Materials

• 1.5ml microcentrifuge tubes
• 2ml collection tube
• QIAquick columns
• Buffer PB
• Buffer EB
• Buffer PE
• DNA mixture from PCR

Protocol

1. Add 5 volumes of Buffer PB to 1 volume of PCR product.
2. Put a QIAquick spin column into a 2ml collection tube.
3. Apply the mixture to the QIAquick column to bind the DNA and centrifuge for 30 to 60 seconds.
4. Discard flow-through. Add 0.75 ml of Buffer PE to the spin column to wash and centrifuge for 30 to 60 seconds.
5. Discard flow-through and centrifuge for another 1 minute.
6. Place QIAquick spin column into a clean 1.5ml microcentrifuge tube.
7. Add 50 µl Buffer EB to the center of the membrane of spin column and centrifuge for 1 minute.
8. If analysing purified DNA using gel, add 1 volume of Loading Dye to 5 volumes of DNA.