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        Desalting Oligonucleotides by Ethanol Precipitation

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        Desalting Oligonucleotides by Ethanol Precipitation

        1. Measure the volume of the oligonucleotide solution to be precipitated.
        2. Chill 95% Ethanol in the freezer at -20 °C or on dry ice prior to use.
        3. Perform Calculations:

          Volume of 3 Molar Sodium Acetate pH 5.2 = 0.1 * Volume of Oligonucleotide Solution

          Volume of 95% Ethanol = 2.5 * (Volume of Oligonucleotide Solution + Volume of 3 Molar Sodium Acetate pH 5.2)

        4. Add the calculated volume of 3 Molar Sodium Acetate to the oligonucleotide solution and vortex for 10 seconds to mix.
        5. Add the calculated volume of 95% Ethanol to the oligonucleotide solution and vortex for 10 seconds to mix.
        6. Place the reaction mixture in the freezer at -20 °C or on dry ice for at least 1 hour.
        7. Centrifuge the reaction mixture to pellet the precipitated oligonucleotide. A small, gray pellet should now be visible in the bottom of the tube.
        8. Pipette off the supernatant and discard.
        9. Add the same volume of cold 95% Ethanol to the pellet and vortex. It is important to break up the pellet to sufficiently wash out trapped salts.
        10. Repeat Step 7 through 9 once more.

          Desalting Oligonucleotides by Ethanol Precipitation

          1. Measure the volume of the oligonucleotide solution to be precipitated.
          2. Chill 95% Ethanol in the freezer at -20 °C or on dry ice prior to use.
          3. Perform Calculations:

            Volume of 3 Molar Sodium Acetate pH 5.2 = 0.1 * Volume of Oligonucleotide Solution

            Volume of 95% Ethanol = 2.5 * (Volume of Oligonucleotide Solution + Volume of 3 Molar Sodium Acetate pH 5.2)

          4. Add the calculated volume of 3 Molar Sodium Acetate to the oligonucleotide solution and vortex for 10 seconds to mix.
          5. Add the calculated volume of 95% Ethanol to the oligonucleotide solution and vortex for 10 seconds to mix.
          6. Place the reaction mixture in the freezer at -20 °C or on dry ice for at least 1 hour.
          7. Centrifuge the reaction mixture to pellet the precipitated oligonucleotide. A small, gray pellet should now be visible in the bottom of the tube.
          8. Pipette off the supernatant and discard.
          9. Add the same volume of cold 95% Ethanol to the pellet and vortex. It is important to break up the pellet to sufficiently wash out trapped salts.
          10. Repeat Step 7 through 9 once more.

         

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