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Resuspending Dried DNA

Objective

Author(s): Pattarin Blanchard

Resuspend DNA oligos and fragments for use in downstream cloning experiments.

Resources

Materials

Procedure

Resuspension into storage stocks

  1. Briefly centrifuge plates at 2000 RPM for 5 seconds (setting is not too important) to make sure pellets are at the bottom of wells.
  2. Calculate how much TE buffer should be added to each well to properly resuspend plates. Add TE buffer accordingly and pipette up and down to resuspend.
    1. Primers (if in pairs, this applies for each individual one) should be resuspended to 100 uM for a storage/master stock.
    2. Fragments, amount depends on yield/manufacturer
      1. Twist normalizes yield to 1000 ng, resuspend in 20 uL TE buffer for a storage concentration of 50 ng/uL
      2. Genscript normalizes yield to 500 ng, resuspend in 10 uL TE buffer for a storage concentration of 50 ng/uL.
      3. IDT depends on fragment length
        1. For fragments up to 750 bp, resuspend in 10 uL TE buffer for a storage concentration of 25-50 ng/uL
        2. For fragments above 750 bp, resuspend in 20 uL TE buffer for a storage concentration of 50 ng/uL
    3. Note: a relatively high stock concentration is desired to minimize freeze-thaw cycles on the storage stocks.

Making working stocks

  1. For each fragment desired, calculate how much storage stock and water are needed to make a diluted aliquot (working stock) such that it is a convenient volume to work with.
    1. Both Golden Gate and Gibson Assemblies typically require 0.05 pmol per fragment, choose a concentration that allows 0.5-1 uL of working stock to be used each time. Keep in mind a typical reaction volume is 15 uL for GGA, 20 for Gibson.
    2. Aim for a volume such that the working stock does not go through more than 10 freeze-thaw cycles to avoid DNA degradation.
  2. In PCR tubes or microcentrifuge tubes, use molecular water to make aliquots, and label appropriately.