Investigating CSI – Background material Table of Contents I ...

• purify DNA from any type of agarose;
• concentrate DNA (for changing buffer, desalting);
• remove proteins (after restriction enzyme treatment; dephosporylation with
BAP or CIAP);
• remove unincorporated nucleotides, primer, primer-dimers and enzymes
from a labeling reaction or PCR;
• remove an excess of linkers after ligation;
• remove residual phenol, chloroform, and ethidium bromide.
• purify plasmid DNA free of RNA from bacterial lysates.
Source: http://herpesvirus.tripod.com/research/protoDNA.htm
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