Talk:'Round-the-horn site-directed mutagenesis

I would not recommend using desalted primers for this procedure, even if they are relatively short (~20 bp each)- I did so and got 1, 2, and 3 base pair deletions at the ligation site. I sequenced 10 constructs and they were all like this, presumably due to truncated primers. Maybe add a warning to use purified primers? This needs to be factored into the tradeoffs for this method. Quikchange works quite well with deslated primers in my hands, probably because the mutation is in the middle of the primer. --Jonathan Lake 12:19, 17 May 2010 (EDT)