The DeNovix® DS-11 Series Spectrophotometer / Fluorometer enables precise absorbance and fluorescence quantification across a wide dynamic range. The dual mode spectrophotometer is equipped with SmartPath® Technology, which facilitates accurate and reproducible measurements for both cuvette and 1 μL absorbance modes. The proprietary optical core of the fluorescence component utilizes LED excitation sources and highly sensitive photodiodes capable of detecting minute amounts of fluorescence across four wavelength ranges.
The purpose of this document is to describe and compare the complementary methods of absorbance and fluorescence quantification.
Basics of Absorbance Measurements
UV-Vis absorbance measurements have long been a standard method for quantification of purified biomolecules in the life science laboratory. This method allows for the rapid detection of molecules based on their absorbance profiles at specific wavelengths.
Absorbance also provides an indication of sample contamination. The shape of the absorbance spectrum will change based on the presence of other molecules that absorb at or near the same wavelengths as the molecule of interest.
Basics of Fluorescence Quantification
Fluorophores are molecules that absorb light at one wavelength (excitation wavelength) and emit light at another (emission wavelength). Certain fluorophores’ structures can be manipulated to fluoresce only when bound to a specific molecule (e.g., double-stranded DNA). Fluorescence assays use this binding specificity to establish a direct correlation between the amount of fluorescence emitted by a sample and the concentration of the biomolecule of interest in solution.
By mixing a fluorophore with a sample of known concentration and measuring the Relative Fluorescent Units (RFU), a relationship between concentration and measured RFU can be plotted and used as a standard curve. The emission of the same fluorophore, bound to unknown samples, can then be plotted against this standard curve to determine the sample concentration.
Comparing Absorbance and Fluorescence Results
When comparing results from absorbance-based methods to fluorescence-based methods, it is important to consider the specificity of each method. Absorbance measurements at 260 nm, for example, are not selective for dsDNA since ssDNA and RNA also absorb at 260 nm. Any absorbance measurement at 260 nm will be a measure of all nucleic acids in a sample and any contaminants that are present, including proteins. This is true for all types of measurements, not just nucleic acids. Absorbance methods are well-suited to measuring pure samples for this reason.
In contrast, fluorescence assays are highly specific for a given species, including but not limited to dsDNA, ssDNA, RNA and proteins. Generally, the concentration of a sample measured by absorbance is greater than the concentration measured by fluorescence methods.
Absorbance vs. Fluorescence Methods
Advantages of absorbance measurements include:
- Reagents are not required. The measured absorbance is a direct result of the molecule of interest absorbing light at a known wavelength.
- The amount of light absorbed corresponds directly to the concentration of the molecule of interest.
In contrast, fluorescence is an indirect measurement.
Advantages of fluorescence include:
- High Sensitivity: Due to the high extinction coefficient of the fluorophore, fluorescence assays are extremely sensitive, allowing for the detection of molecules at concentrations hundreds of times lower than what is detectable by traditional absorbance.
- Specificity: The binding properties of the fluorophore make these methods highly selective for specific molecules. These assays are ideal for samples that may contain contaminants that would interfere with an absorbance measurement.
Absorbance and fluorescence are distinct but complementary methods of quantitation. Quantitation via absorbance using the microvolume or cuvette based capabilities of the DS-11 Series is ideal for the rapid and accurate measurement of purified samples, including nucleic acids and proteins.
Fluorescence quantitation, using a secondary reporter fluorophore, is ideal for samples that fall below the detectable threshold for UV-Vis absorbance. In some cases, fluorescence quantitation methods can also be used to detect samples in the presence of contaminants or buffer elements that would interfere with UV-Vis measurements.
The DS-11 Series Spectrophotometer / Fluorometer integrates UV-Vis and fluorescence capabilities in a small bench top footprint. DeNovix offers several instrument models with combinations of microvolume absorbance, cuvette absorbance and fluorescence measurement modes. Both absorbance and fluorescence methods share the same EasyApps® software and sample export features, making data analysis fast, easy and intuitive.