problem in cloning PCR primer design with restriction site
Posted 12 March 2013 - 10:35 AM
Im designing a primer pair for amplification and cloning and expression in pET expression plasmid. I have chosen Nde1 and Xho1 restriction sites for the purpose.First i have taken the gene to be cloned and designed a primer pair as described below
1. Forward primer - length 22 bp, Tm - 54, GC - 27 %
2. Reverse primer - length 22 bp ,Tm - 52 GC - 24 %
After adding the restriction site and 6 additional bases (to both primer sets) Tm increases to 74, GC % of the primer set is 35 %
Im unable to get good primer pair
Posted 12 March 2013 - 11:19 AM
Posted 12 March 2013 - 04:36 PM
With your low GC, you should also consider lowering your extension (not the annealing) temperature, perhaps to 64 rather than 72, and doubling the extension time. This will allow you to PCR very low GC regions, which otherwise cannot be extended.
Posted 26 March 2013 - 04:27 PM
I think you are doing fine. the new parameters for the primers look fine, as long as the two primers do not have a big difference in Tm. Another thing is you don't necessarily need to add 6 nt to the end of the primers, some restriction enzymes require less extra bases. You can take a look here: [url="https://www.neb.com/tools-and-resources/usage-guidelines/cleavage-close-to-the-end-of-dna-fragments"][url]https://www.neb.com/...f-dna-fragments[/url][/url]
So restriction enzymes won't cut dsDNA fragments unless they're flanked by at lest 1 bp beyond the restriction enzyme recognition site?