Primers
- How does SnapGene estimate oligonucleotide (primer) melting temperatures (Tm)?
- Can I configure SnapGene to show primer Tm values suitable for PCR polymerases such as Phusion®, Phire®, and Q5®?
- I have a list of primers in an Excel file. Can I import those primers into SnapGene?
- My primer shows up at irrelevant binding sites, or does not show up at the binding sites of interest. How can I adjust the number of binding sites?
- What is the Red Squiggle I See When I Create or Edit a Primer?