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BIOTEC Dresden/Notepad/18 August 2010
From 2010.igem.org
The PCR products from the backbone amplification experiment were digested with DpnI restriction enzyme for 4 hours followed by heat inactivation.
Digestion was followed by a second purification with the pcr purification kit, concentration determination with nanodrop (today: in the range 60-80 not much lower than before digestion) and finally by running the samples on an agarose gel (although detectable, the band seemed rather weak and was accompanied by a smear)
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