Get Help Sign In

Frequently asked questions

Our Scientific Applications Support team has assembled a list of frequently asked questions to help you find answers quickly. Filter using one or more categories to focus on specific topics, or use the search bar to perform a text search.

How do I use the OligoAnalyzer tool to analyze possible hairpins and dimers formed by my oligo?

To do hairpin or dimer analysis, click on the appropriate option to the right of your sequence. For hairpin analysis, you can change the default concentrations provided to match your reaction conditions.

The most valuable piece of information on this screen is the Tm for each of your structures. If the Tm of the structure is lower than your reaction conditions, then this structure will not cause any problems. If it is higher, this oligo may be problematic and should be redesigned. For self-dimer analysis, click on 'Self-Dimer' to bring up a new window with each possible self-dimer your oligo can form.

For each diagram you will be able to see the calculated delta G value for this secondary structure. If you have a strong delta G (-9kcal/mol or more negative) this oligo could be problematic. Heterodimer analysis works the same way as self-dimer analysis. Use the ""Hetero-Dimer"" button in the OligoAnaylzer® program to test for primer dimers.

Enter the sequence of your forward primer into the sequence box, and then click 'Hetero-Dimer.' This will open a second box below the original sequence box, in which you enter the sequence of your reverse primer.

Then click the ""Calculate"" button below the second box. In general, a primer pair with a delta G of -9kcal/mol or more negative will be problematic.

Custom DNA & RNA