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Annealing oligonucleotides

Use this quick protocol for making double-stranded DNA from single-stranded, complementary oligonucleotides. Also review some considerations for making and using annealed oligos.

Jun 15, 2012

It is sometimes necessary to make double-stranded DNA from single-stranded, complementary oligonucleotides. While the annealing procedure is fairly straightforward, attention to a few details can greatly reduce the presence of undesired single-stranded material.

Protocol

  1. Resuspend. After briefly spinning down each oligonucleotide pellet, dissolve in Duplex Buffer (100 mM Potassium Acetate; 30 mM HEPES, pH 7.5; available from IDT)—this provides a buffering environment and the salt is necessary for oligonucleotide hybridization. Dissolve each oligo at high concentration (1–10 OD260/100 μL); see Table 1 for guidelines on resuspension volumes. Heating (up to 94°C) and vortexing will facilitate resuspension.
  2. Mix. Add the 2 oligo strands together in equal molar amounts. This step is critical to avoid residual single-stranded material.
  3. Anneal. Heat the mixed oligonucleotides to 94°C for 2 minutes and gradually cool. For many oligos "cooling" can be as simple as transferring samples from the heat block or water bath to the bench-top at room temperature. For sequences with significant secondary structure, a more gradual cooling/annealing step is beneficial. This is easily done by placing the oligo solution in a water bath or heat block and unplugging/turning off the machine.
  4. (Optional) Dilute. if needed, dilute the annealed oligonucleotides using Nuclease-Free Duplex Buffer or 1X IDTE Buffer.
  5. Store. The resulting product will be in a stable, double-stranded form and can be stored at 4°C or frozen.

Table 1. Recommended resuspension volumes.

PT_Annealing oligos_Table 1

    Things to consider:

    Avoiding contamination and degradation—If you plan to use the duplex on multiple occasions, divide it into smaller aliquots and store at –20°C. Nuclease-free Duplex Buffer is available from IDT and is certified nuclease-free by testing with IDT RNaseAlert and DNaseAlert™ Kits. Find out more about these products at www.idtdna.com.

    Secondary structure—Low yields of the expected, annealed product can be caused by secondary structure. Use the OligoAnalyzer® program (www.idtdna.com/scitools) to determine whether there is significant secondary structure in the oligonucleotides. Problematic annealing can often be resolved by slow cooling, as described in Step 3, above.

    Ligation—If the double-stranded oligonucleotide product will be used in a ligation reaction, you may need to add 5’-phosphates to the strand ends. These can be added at the time of oligo synthesis (chemical phosphorylation; done by request) or anytime thereafter (before or after annealing) using polynucleotide kinase (enzymatic phosphorylation).

    Cloning—If the resulting double-stranded DNA fragment will be relatively long (>60 bp), or will be used in cloning, we recommend starting with PAGE-purified oligos (IDT can provide this service).

    Annealing RNA—The IDT research team also uses this protocol to create siRNA duplexes from single-stranded, complementary RNA oligos.

    Let us anneal your oligos for you!

    For a small fee, IDT will anneal your oligos for you, so that you can proceed with your experiments as soon as your oligos arrive. To request this Duplex Service, go to the Duplex Entry page.

    For additional information, please contact the IDT Technical Support Group at applicationsupport@idtdna.com.

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