August 19, 2011 -- RapidTip based PCR purification for sanger sequencing applications results in the retention of dNTPs, primers and primer dimers of <50bp inside the tip, while repelling the double stranded DNA targets (such as PCR amplicons) to remain in solution, in just 60 seconds. No more tedious bind-wash-elute, magnetic beads or enzymatic based protocols are required to obtain excellent yield with an environmentally friendly disposable tip.
More information contact:
Grazie Mendonsa, Ph.D.
800-227-9997
Grazie.Mendonsa@midsci.com
