Oligo resuspension calculator
Work out the volume of buffer to add to a dried oligo to reach a target stock concentration, from the amount supplied in nmol.
How it works
Formula
volume = amount ÷ concentration. With amount in nmol and concentration in µM, volume (µL) = (nmol ÷ µM) × 1000. A handy shortcut: for a 100 µM stock, µL = nmol × 10.
Worked example
A 10 nmol oligo to 100 µM: (10 ÷ 100) × 1000 = 100 µL. Checking: 10 nmol in 100 µL = 100 µmol/L = 100 µM.
When to use it
When resuspending a freshly synthesised, lyophilised oligo to a known stock concentration before making working dilutions for PCR or sequencing.
Sensible defaults
Defaults resuspend a typical 10 nmol synthesis to a 100 µM stock (→ 100 µL). Read the exact nmol delivered from your oligo spec sheet.
FAQ
- Where do I find the nmol amount?
- On the oligo synthesis spec sheet from the vendor — it lists the actual nmol (or OD/µg) delivered, which varies per synthesis.
- What concentration should I resuspend to?
- A 100 µM stock is common; you then dilute to a 10 µM working stock for most PCR. Pick whatever your protocol expects.