DNA Concentration Calculator

Knowing the concentration of the DNA in a sample is fundamental in many experiments and laboratory techniques: with our DNA concentration calculator, you will learn how to determine that quantity using the absorbance.

Here you will learn:

• What is DNA concentration, and how do we calculate it;
• How to calculate the DNA concentration from A₂₆₀ values;
• The DNA concentration equation (both for nucleic acid samples and oligonucleotides).

The measurement of the concentration of DNA (or RNA) is obtained through various techniques: the choice depends on the desired sensitivity or purposes. Our DNA concentration calculator will analyze the spectrophotometric technique, commonly used since it doesn't require additional reagents and its relative simplicity, it lacks sensitivity at low concentrations, and it can't distinguish between the two nucleic acids.

The only instrument required for the measurement of the DNA concentration is a spectrophotometer. Place the sample in a quartz cuvette, and measure its absorbance at the ultraviolet wavelength of $260\ \text{nm}$: we call this quantity $\text{A}_{260}$.

The calculation of the DNA concentration from A₂₆₀ values uses the Beer-Lambert Law. The equation for the DNA concentration is:

Here we can identify:

• $c_{\text{DNA}}$, the DNA concentration;
• $b$, the length of the optical path;
• $\text{df}$, the dilution factor; and
• $c$, the conversion factor.

The conversion factor depends on the type of nucleic acid under analysis. Its value is:

• $33\ \text{µg}/\text{mL}$ for single-stranded DNA (ssDNA);
• $50\ \text{µg}/\text{mL}$ for double-stranded DNA (dsDNA); and
• $40\ \text{µg}/\text{mL}$ for RNA.

The dilution factor is nothing but a measurement of the quantity of acid nucleic per unit volume of water.

The formula for the DNA concentration can be slightly modified to consider any short sequence of nucleotides (oligonucleotide), given that we know the composition of the sequence.

Where we introduced the quantity:

• $e_{260}$, the extinction coefficient; and
• $w_{\text{M}}$, the molecular weight of the nucleotide strand.

To compute the molecular weight of the oligonucleotide, sum the weights of the nucleotides making up the sequence. First, use the data in the following table:

The weights are expressed in Daltons, a unit defined by $$\text{N}{\text{A}}\ \text{Da}\simeq 1\ \text{g}/\text{mol}$where$\text{N}{\text{A}}$$ is the Avogadro's number.

To refine the calculations for the weight of the oligonucleotide, you need to apply the following modifications:

• Subtract $61.96\ \text{Da}$ for ssDNA or $123.38\ \text{Da}$ for dsDNA if you are using unmodified nucleotides.
• Add $17.04\ \text{Da}$ for ssDNA or $34.08\ \text{Da}$ for dsDNA in nucleic acids with added phosphate groups.

*Add $159.0\ \text{Da}$ for RNA with added phosphate groups.

To calculate the absorption coefficient $\epsilon_{260}$ at $260\ \text{nm}$, we use the nearest neighbour model for nucleotides. Use the formula:

And substitute the vales of absorption for the individual basis:

And for the nearest neighbour in the 5'/3' direction, use the following table:

Use these values (expressed in M^-1cm^-1, the inverse of molarity per centimeter) in the DNA concentration formula to calculate the value of the DNA concentration from A₂₆₀ values also in short sequences of nucleotides.