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How does one re-suspend DNA oligos?

How does one re-suspend DNA oligos?

DNA kept frozen in a nuclease-free environment should be stable for years. One will find it convenient to initially make a freezer stock (which should be thawed relatively infrequently) at 100uM concentration. Adding a volume a TE (uL) equal to ten times the number of nanomoles of DNA present in the tube (as noted on the spec sheet provided with the oligo) will produce a stock solution at this concentration.

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