DNA Base Pair Calculator

Convert between base pairs (bp) and physical length, compute molecular weight (g·mol⁻¹), moles and copy number, or paste a sequence for quick stats (length, GC%). Supports custom parameters for rise per bp and avg. mass per bp.

Length ⇄ Base pairs

Use the two fields (bp or length) — leave the one to compute blank and click Solve.

DNA base pairs: physical length, molecular weight, copy number and practical notes

This tool helps convert DNA base pairs into physical lengths and molecular masses, compute moles and copy numbers, and provides quick sequence statistics like GC percentage. It is designed for bench biologists, students and bioengineers who need fast, reliable conversions for cloning, PCR and quantitation.

1. Rise per base pair and assumptions

B-form double-stranded DNA (the common conformation under physiological conditions) has a rise per base pair of approximately 0.34 nm (3.4 Å) and ~10.5 bp per helical turn. These are average values — local sequence, supercoiling, and binding proteins can alter local geometry. The calculator uses 0.34 nm/bp by default but you can override it in Custom Parameters.

2. Molar mass per base pair

The average molar mass per base pair for double-stranded DNA is commonly approximated as 660 g·mol⁻¹ per bp. This average accounts for the four nucleotides plus the sugar-phosphate backbone. For single-stranded DNA or precise mass calculations (when exact sequence composition is known), compute nucleotide-level masses instead — the sequence tab provides a coarse estimate using 660 g·mol⁻¹ per bp.

3. Copy number, Avogadro and mass conversions

Given a DNA length (bp) and mass (e.g., ng), you can compute the number of molecules (copies) using:

copies = (mass (g) / molar_mass (g·mol⁻¹)) × N_A

where N_A = Avogadro's number = 6.02214076×10²³ mol⁻¹. The calculator handles unit conversions (ng, µg, mg, g) automatically.

4. Worked examples

Example 1 — plasmid length: A 3000 bp plasmid has physical length ≈ 3000 × 0.34 nm = 1020 nm = 1.02 µm — useful for visualisation or gel expectations.

Example 2 — copy number: A 5000 bp PCR product with mass 10 ng — molar mass ≈ 5000 × 660 g·mol⁻¹ = 3.30×10⁶ g·mol⁻¹. Number of moles in 10 ng = 1e-8 g / 3.30×10⁶ g·mol⁻¹ ≈ 3.03×10⁻¹⁵ mol. Copies ≈ 3.03×10⁻¹⁵ × 6.022×10²³ ≈ 1.82×10⁹ molecules.

5. Sequence-based mass & GC%

Pasting a sequence provides exact bp count and GC percentage. For more accurate mass per mole use sequence-specific nucleotide masses (A/T/G/C) if available — this tool uses the average 660 g·mol⁻¹ per bp for quick estimates.

6. Practical tips

  • For molar calculations and qPCR standards, be explicit about whether your DNA is double-stranded or single-stranded; single-stranded DNA molar mass per nucleotide is lower.
  • When preparing standards, account for salt and buffer mass if measuring by weight — purified DNA mass may include residual salts/contaminants.
  • Use spectrophotometric (A260) or fluorometric (PicoGreen) quantitation depending on sensitivity and contaminants.

7. Precision and rounding

The calculator performs conversions in double precision internally; choose display precision for reporting. For low-copy-number work, keep more significant digits in intermediate steps to avoid rounding error.

8. Limitations

Average approximations (0.34 nm/bp, 660 g·mol⁻¹ per bp) are convenient but not exact. When analyzing oligonucleotides or exact plasmid sequences for quantitative work, use sequence-specific monoisotopic masses or the exact nucleotide composition.

9. Summary

Use this tool to quickly convert between bp and length, compute masses and copy numbers, and get fast sequence stats. Toggle custom parameters if you need different assumptions, and export CSV for lab records.

Frequently Asked Questions

1. What rise per bp should I use?
Default 0.34 nm/bp for B-DNA is standard. For A- or Z-DNA or stretched DNA, use measured or literature values via Custom Parameters.
2. Why 660 g·mol⁻¹ per bp?
660 g·mol⁻¹ per bp is an empirical average for dsDNA; use nucleotide-specific masses for greater accuracy.
3. How do I compute copy number?
Copies = (mass (g) / molar mass (g·mol⁻¹)) × Avogadro's number. This calculator does that automatically in Mass mode.
4. Can I input single-stranded DNA?
Yes — but note average mass per nucleotide differs; adjust Custom Parameters accordingly.
5. Does the sequence analyzer validate characters?
Non-ATGC characters are ignored and a warning is shown; only A/T/G/C are counted.
6. Can I export results?
Yes — use the Download CSV button to export computed values and derivations for lab records.
7. Is length calculated for linear DNA only?
Yes — circular DNA physical contour length matches linear length in nm/µm, but topology (supercoiling) affects apparent properties like electrophoretic mobility.
8. How accurate are copy-number estimates?
Accuracy depends on mass measurement method and assumptions about purity and double-strandedness. Fluorometric assays tend to be more accurate than absorbance for low concentrations.
9. Can I change Avogadro's number?
Avogadro's number is fixed as 6.02214076×10²³ mol⁻¹ in this calculator; change only for hypothetical analyses by editing the source code if needed.
10. How should I prepare standards?
Prepare standards by mass or molarity with known purity; prefer plasmid linearization for consistent behavior in qPCR standards.