DNA Concentration Measurement At 260 nm Using Photopette® Bio

Download this  Application Note as PDF File here: AN-LS-001 – DNA Concentration Measurement At 260 nm Using Photopette® Bio

A. Lee, Acumen Research Laboratories Pte Ltd, Singapore and A. Jain, Tip Biosystems Pte Ltd, Singapore

– Photopette Bio makes measurement of DNA concentration efficient.
– Sample purity (A260/A280) could be measured concurrently

Objective: The objective of this application note is to demonstrate how Photopette Bio can be used for direct DNA concentration measurement and DNA purity for unknown samples. Furthermore, it acts as a handy guide to get you started with Photopette, and outlines application-specific parameters for reference.


DNA (deoxyribonucleic acid) concentration measurement is a commonly performed procedure in life science and biomedical research laboratories. A spectrophotometer is able to determine DNA concentration as well as its purity [1]. It is based on the principles that nucleic acids absorb ultraviolet (UV) light at a specific wavelength. For pure DNA samples, the maximum absorbance occurs over a broad peak at around 260 nm; at 280 nm it only absorbs about half as much UV light compared to 260 nm [2]. DNA absorbs UV light due to heterocyclic rings of the nucleotides, its sugarphosphate backbone does not contribute to this absorption [3]. Factors such as pH and ionic strength can further affect the absorbance spectrum. Typical spectrums of UV absorbance for different concentrations of purified DNA are presented in Figure 1.

The DNA concentration of an unknown sample can be determined at a wavelength of 260 nm using Beer-Lambert Law. The method does not require any other additional reagents or preparations, or the generation of a standard curve in advance. The ratio of the absorbance at 260 nm and at 280 nm (A260/A280) is used to assess purity of the DNA sample. This approach is only useful for pure DNA samples. Impurities such as protein, RNA and insoluble cell lysate factors also absorb in similar UV range and therefore, could in interfere. A260/A280 for a pure DNA sample is usually about 1.8 [2]. Since pure RNA has an A260/A280 ratio of 2.0, a DNA sample with A260/A280 ratio greater than 1.8 suggests RNA contamination [4].


– Photopette® Bio (260, 280, 340 nm)

– Human DNA Quantitation Standard (NIST SRM372)
– Tris-EDTA buffer (Sigma Aldrich #93283)

Fig. 1:UV absorbance spectrums for different DNA concentrations


Highlighted in this section are the steps followed to perform measurement for DNA standards. It is advised to perform an application specific risk-assessment analysis before performing an experiment. Please refer to the Photopette User Manual for operating and safety precautions [5].


Turn-on the Photopette device and connect to the Photopette iOS/Android app. Select ‘ssDNA’ or ‘dsDNA’ as the measurement type, depending upon the sample type. Select dataset and set additional settings (if needed) before selecting ‘Start Measurement’. Please follow the videotutorials available online at www.tipbiosystems.com to get familiar with the measurement process.

Tris-EDTA buffer (TE buffer) can be used as blank sample. A CuveTipTM was mounted on the Photopette and it was dipped in the blank sample to perform auto-zero measurement. Please ensure that there is no air-bubble trapped in the CuveTip Cavity. Note: Presence of air-bubbles may disrupt the optical path and will lead to inaccurate measurements.

Subsequently, DNA solutions with different concentrations were prepared by serial dilutions using TE buffer. DNA concentration was calculated based on the information provided in NIST SRM certificate of analysis [6]. For each concentration, five replicates were taken. Measurement results for 260 nm are tabulated in Table 1.

Table: Absorbance values for prepared DNA standards


The data was used for generation of a standard curve, and to determine experimental parameters such as limit of detection, linear range and dynamic range. The absorbance values in Table 1 were plotted in the Figure 2.


Upper measurement-limit and linear range:
Based on dynamic range From Figure 2, we can deduce that the upper measurement-limit for DNA measurements is beyond 50 ng/µl. Regression analysis indicates the linear range to be beyond 50 ng/µl as well.

Sample purity and A260/A280 ratio:
The absorbance values for 260 nm and 280 nm are tabulated below in Table 2. A260/A280 ratio (i.e. ratio for sample purity) was thus calculated and highlighted in adjacent column.

The recommended absorbance range starts at 0.1 AU, thus measurement readings below 0.1 AU were ignored and are highlighted in red in the Table 2. The A260/A280 ratio is highly sensitive to the peak wavelength and bandwidth for 260 nm and 280 nm [7]. Since Photopette relies on LED technology, the peak wavelength tolerance and bandwidth is higher. Therefore, the ratio of about 2.5 should be used as the purity.

Fig. 2: Absorbance value plot for the prepared turbidity standards
Table 2: Absorbance values for prepared DNA standards and their purity ratio.


A standard curve was plotted in Figure 3 for data within 2 ng/μl to 50 ng/μl. A linear regression was performed on the data using Microsoft’s Excel® software, and a linear fit was performed. The equation of standard curve along with its R-squared value was obtained. The slope of the linear component of the standard curve is 0.012 AU μl/ng.

Photopette users may download a pre-configured worksheet for the DNA measurement from our ‘online resource section’. The worksheet is compatible with Microsoft Excel® and similar worksheet software, and will aid users in performing the calculations and generating the standard curve.

Limit of Detection

The Limit of Detection (LOD) for this assay using Photopette is determined by factoring in the standard-deviation for blank measurements as well as experimental data using the equation given below:

LOD = 3 x SDblank / Slope(Standard Curve)

Standard Deviation for blank measurements with 50 repeats using same CuveTip was found to be 0.005 AU. Thus, the limit of detection for the DNA measurement with Photopette using the equation above was 1.25 ng/μl.

LOD = 3 x (0.005 AU) / (0.012 AU μl/ng) = 1.25 ng/μl


It is important that the DNA sample to be measured using this approach should be pure in order to avoid other interfering biological entities and proteins.


The application note guides the user for determining DNA concentration in a given sample. It highlights experimental parameters such as limit of detection, upper measurement limit and linear range for such measurements.


[1]“Understanding and measuring variations in DNA sample quality.” [Online]. Available: https://www.ogt.com/resources/literature/483_und erstanding_and_measuring_variations_in_dna_sam ple_quality. [Dated: 30-Mar-2017].

[2]Rothman R., “Determination of DNA Concentration and Purity by Ultraviolet Spectrophotometry.”

[3]H. F. Lodish, Molecular cell biology. W.H. Freeman, 1999.

[4]“Thermo Scientific NanoDrop Spectrophotometers Protein A280 Protein A280 Protein A280,” 2010.

[5]Tip Biosystems, F. Omar, “Photopette User Manual V1.0.0,” Singapore, 2016.

[6]“Certificate of Analysis.” NIST Humanzied DNA Standard.

[7]“T042 – Assessment of Nucleic Acid Purity.”

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