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.

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How do I separate double-stranded from single-stranded oligos while still getting good recovery?

The best way to distinguish and separate double-stranded oligonucleotides from those that are single-stranded is by running them on a non-denaturing electrophoresis gel. At IDT, we would use a 12-15% polyacrylamide, 1X TBE gel. The lack of denaturants (e.g., urea, SDS) keeps the double-standed oligos intact. You can then excise this product band from the gel and extract the oligonucleotides from it. Please note, however, that no matter how careful you are, you will lose some yield during the extraction process. Electrolution will return the most full length product from the gel. Though, not quite a effective as electroelution, dialysis can also be used. For additional information on electrophoresis protocols, visit www.protocol-online.net.

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Custom DNA & RNA