Resuspension Calculator

Calculate the solvent volume needed to resuspend a known nanomole amount at a target micromolar concentration.

Oligo and compound resuspension
Enter the dry amount in nanomoles and the desired stock concentration in micromolar.

About resuspension calculations

Resuspension turns a measured dry material into a liquid stock solution by adding a suitable solvent. In molecular biology and chemistry laboratories, synthesized oligonucleotides, primers, probes, peptides, and small compounds often arrive as a dry pellet or film with the amount reported in nanomoles. Choosing the solvent volume from the desired concentration makes subsequent pipetting and dilution straightforward. This calculator uses the relationship concentration equals amount divided by volume. With amount entered in nanomoles and target concentration in micromolar, the convenient laboratory conversion is volume in microliters = amount in nanomoles × 1,000 divided by concentration in micromolar. The factor of 1,000 reconciles the metric prefixes. For example, 25 nmol prepared at 100 µM requires 250 µL of solvent. The result is the final solution volume, which is normally approximated by the volume added when the dry material contributes negligible volume. Target concentration should be selected for the downstream workflow. A 100 µM stock is common for DNA primers because simple tenfold dilutions produce 10 µM working stocks, but the appropriate value depends on assay design, stability, solubility, and laboratory protocol. Very small calculated volumes may be difficult to pipette accurately. In that situation, prepare a lower concentration or use a staged dilution rather than relying on a volume below the reliable range of the available pipette. Solvent choice matters as much as arithmetic. Nuclease-free water or a suitable buffered solution may be recommended for oligonucleotides, while other compounds can require a specific aqueous buffer or organic solvent. Follow the supplier's handling instructions, including pH, mixing, temperature, light protection, storage, and freeze-thaw guidance. Confirm that the material is soluble at the chosen target concentration before preparing the stock. After adding solvent, mix using the method appropriate for the material and allow enough time for complete dissolution. Brief centrifugation can collect liquid from tube walls. Label the stock with identity, concentration, solvent, preparation date, and storage conditions. The calculation assumes the supplier's stated nanomole amount is correct and that all material dissolves. For critical quantitative work, account for purity, water content, salt form, recovery, and any concentration verification recommended by the laboratory method.

Resuspension examples

The examples convert nanomoles and micromolar targets directly to microliters.

Dry amount and targetAdd solventCalculation
25 nmol at 100 µM250 µLMultiply 25 by 1,000 and divide by 100.
7.5 nmol at 50 µM150 µLA lower target concentration requires a larger solvent volume.
40 nmol at 200 µM200 µLThe higher concentration keeps the final stock volume compact.

How to calculate a resuspension volume

  1. Find the dry material amount in nanomoles on the supplier label or certificate.
  2. Choose a target stock concentration in micromolar that suits the downstream protocol.
  3. Enter both positive values using the displayed units.
  4. Select Calculate resuspension volume and note the solvent volume in microliters.
  5. Confirm solvent compatibility and practical pipetting precision before preparation.

Resuspension calculator FAQ

Why does the formula include a factor of 1,000?

The factor converts the nanomole and micromolar inputs into a microliter volume. It follows directly from the metric relationships between moles, nanomoles, liters, and microliters.

What solvent should I use?

Use the solvent recommended by the material supplier or laboratory protocol. Solubility, stability, pH, nuclease control, and downstream compatibility can all affect the correct choice.

Is 100 µM always the best stock concentration?

No, although 100 µM is common for oligonucleotide stocks. Select a concentration that is soluble, stable, and convenient for the required working dilutions.

What if the calculated volume is too small to pipette?

Choose a lower target concentration to increase the solvent volume or use an appropriate staged preparation. Do not assume a pipette remains accurate below its specified operating range.

Does the dry material change the final volume?

The calculation treats its volume contribution as negligible, which is usually reasonable for small dry amounts. More exact preparations should be brought to a defined final volume rather than simply adding that volume of solvent.