From sequence to amount
Enter the sequence as plain text or one FASTA record. Spaces, line breaks and lowercase letters work. Choose DNA or RNA explicitly: T is not silently changed into U. Ambiguous bases, numbers and modification labels are refused.
For double-stranded DNA, enter just one strand. The other is its exact complement; the calculation assumes a fully paired, blunt-ended duplex with hydroxyl ends. It does not describe a circular plasmid, a restriction fragment with phosphate ends, or a pair with overhangs.
How molecular weight is calculated
Add the nucleotide unit weights, then subtract 61.96 g/mol per strand. The result is an average anhydrous acid-form molar mass, numerically equal to the molecular mass in daltons. It is not a monoisotopic mass or a mass including counterions.
| Nucleotide | DNA unit weight (g/mol) | RNA unit weight (g/mol) |
|---|---|---|
| A | 313.21 | 329.21 |
| C | 289.18 | 305.18 |
| G | 329.21 | 345.21 |
| T / U | 304.20 (T) | 306.17 (U) |
For a known modified-oligo mass, use the molarity calculator. A supplier's product-specific value takes precedence over this unmodified model.
Worked example: M13 forward primer
The single-stranded DNA sequence GTAAAACGACGGCCAGTG has 18 bases and a calculated molar mass of 5,557.68 g/mol. At 5.47 nmol, that corresponds to 30.401 µg, or 30.4 µg rounded.
The conversions use n = m / MW and c = ρ / MW, after bringing mass into grams and volume into litres. For this primer, 10 ng/µL ≈ 1.7993 µM. These are conversions from the entered quantity, not measurements of purity or recovery.
Prepare the next step
Use the delivered amount in the primer resuspension worksheet to find a stock volume and plan a working dilution. Use the primer Tm calculator for the separate temperature calculation with explicit salt and concentration settings.
Sources and assumptions
DNA unit weights and end correction: Glen Research, The Glen Report 34.1 (2022), page 12. RNA unit weights and hydroxyl ends: Eurogentec oligonucleotide FAQ. Checked October 1, 2026.
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