Brief procedure:
※ Principle : mini spin column (silica matrix)
※ Sample size : 1. Wet weight ≦ 100 mg
2. Dry weight ≦ 20 mg
※ Operation time : 30 ~ 60 minutes
※ Binding capacity : up to 60 μg total DNA / column
※ Expected yield : 5 ~ 40 μg /prep
※ Column applicability : centrifugation and vaccum
※ Minimum elution volume : 50 μl
Important Notes :
※ Buffers provided in this system contain irritants. Wear gloves and lab coat when handling these buffers.
※ Check PG1 Buffer before use, Warm PG1 Buffer at 60℃ for 5 min if any precipitate formd.
※ Preheat dry baths or water baths to 65℃ before the operation.
※ Add required ethanol (96-100%) to PG3 Buffer, GW and Wash before use.
※ Store RNase A at -20℃ upon recipit of kit. Add sterile ddH2O to RNase A tube to make a 50 mg/ml stock solution. Vortex and make sure that RNase A has been completely dissolved. Store the stock solution at -20℃ .
※ All centrifuge steps are done at full speed(~ 18,000 x g) in a microcentrifuge.