Basic information about microplate readers
What is a Microplate Reader?
A microplate reader is a laboratory instrument that is used to measure chemical, biological or physical reactions, properties, and analytes within the well of a microplate. A microplate consists of small wells in which separated reactions take place. In the microplate, these reactions convert the presence of an analyte or the progression of biochemical processes into optical signals. The microplate reader detects these signals and thus quantifies the parameter of interest.
Scientists in the life sciences and pharmaceutical industries strive to improve routine laboratory processes and efficiency by using products or instruments able to save time. A microplate reader can handle up to 3456 samples in minutes or even seconds. A plate reader helps to minimise operational time and to save reagent costs, allowing researchers to dedicate more time to data analysis and the generation of actionable insights.
What is a microplate reader used for?
A microplate reader is used for the quantification of several biological and chemical assays in a microplate. Nowadays, the availability of a plethora of reagent kits enables the exploitation of a microplate reader in different fields and for many different applications. Besides biological, cellular, biochemical, pharmaceutical research and drug discovery, both in academic and industrial environments, plate readers are also used in drug discovery, environmental research, and in the food or cosmetics industry.
Working principle of a microplate reader
A microplate reader detects light signals produced by samples that have been pipetted into a microplate. The optical properties of these samples are the result of a biological, chemical, biochemical, or physical reaction. Different analytic reactions result in different optical changes used for analysis. Absorbance, fluorescence intensity, and luminescence are the most popular and most frequently used detected modes in laboratories worldwide. Additionally, advanced modes such as fluorescence polarization, time-resolved fluorescence, and AlphaScreen® are also available on microplate readers.
Microplate based measurements detect light signals produced by a sample, converted by a sample, or transmitted through a sample. In the plate reader, the signal is measured by a detector, usually a photomultiplier tube (PMT). PMTs convert photons into electricity that is then quantified by the microplate reader. The output of this process is numbers by which a sample is quantified.
Depending on the nature of the optical signal changes during a reaction and consequently on the detection mode, samples on a microplate may need to be excited by light at specific wavelengths. This light is usually provided by a broadband xenon flash lamp. To allow excitation of the sample only by specific wavelengths, the light produced by the lamp is selected by a specific excitation filter or monochromator. On microplate readers, to increase sensitivity and specificity, filters or monochromators are equally employed on the emission/detection side. These are usually placed between the microplate and the detector.
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Which assays would I like to do?
When a plate reader is to be procured, there are already applications known that are to be measured. However, it makes sense to pay more attention to this question to find the right and future-proof reader for the laboratory. On the one hand, you will have to run basic assays to quantify biomolecules such as nucleic acids and proteins, or cell viability. For all these applications, several solutions are available that are based on different principles, detection modes, and sensitivities. Therefore, it is important to know in advance the exact name and supplier of the kit or the chemistry you want to use on your plate reader. On the other hand, there are thousands of tests that answer specific biological questions. There may be solutions to problems that you usually solve with cumbersome tests, although simpler solutions based on microplates are available. Therefore, reviewing your day-to-day lab work and gathering information on how colleagues use microplate readers is a fundamental step before you buy a plate reader. Alternatively, you can find countless suggestions on how a microplate reader can simplify your research in our "research areas".
Which detection mode do I need for my assay?
Different assays are detected differently, even though they might answer the same biological question. If you already identified commercial kits, you will find the required detection mode in the product insert. Otherwise, detection modes that are available in a microplate reader and what they are typically used for are described below.
Absorbance measures how much light is lost (absorbed) when transmitted through a sample. Molecules often absorb light at a specific wavelength and can be quantified by measuring their absorbance. Wavelength selection capability is mandatory on an absorbance microplate reader and can be achieved with filters, monochromators or spectrometers. Typical applications that are read by an absorbance microplate reader are:
Fluorescence intensity (incl. FRET)
Fluorescence is the absorption of light energy and its transformation into emission light, next to kinetic energy and heat. Since the emitted light is lower in energy than the input light, emission is always of higher wavelength. The process of energy uptake, energy conversion and light emission is quick and occurs in a nanosecond timeframe. Hence, the detection of fluorescence intensity occurs as follows in a plate reader: excitation with light at a specific wavelength and detection of the emission light at higher wavelength at about the same time. The wavelength selection is accomplished via filters or monochromators. The intensity of fluorescence is linear to the concentration of a fluorophore and is accordingly used to quantify fluorescent (or fluorescently labelled) molecules. Other fluorescence intensity applications employ a shift in fluorescence emission or an increase of fluorescence when interacting with a molecule of interest to detect a specific molecule. Typical fluorescence applications detected by a fluorescence plate reader are the following:
Cell viability assays Resazurin assay, Calcein-AM Aggregation assays Thioflavin T (RT-QuIC) Enzyme activity assays 4-methylumbelliferone (4-MU), NADH-based assays, 7-Amino-4-Methylcoumarin (AMC) Reactive oxygen species H2DCFDA assay, DCF assay Nucleic acid quantification Qubit assays, Quant-iT assays (e.g. PicoGreen)
Luminescence (incl. BRET)
The emission of light without prior excitation is referred to as luminescence. The production of luminescence in life science experiments occurs as the result of a chemical reaction and is either spontaneous or needs enzymatic catalysis. In a spontaneous luminescence reaction, the substrate as well as co-factors need to be present to generate light. For an enzyme-dependent luminescence reaction, a functional enzyme is essential. Such an enzyme is called luciferase. To detect the emitted light of a luminescence assay on a plate reader, a detector is necessary. Typically, all light coming from a well is bundled by a lens and guided to the detector. Accordingly, a luminescence plate reader does not rely on filters or on an excitation source. For dual emission assays, the wavelength selection is accomplished via filters or monochromators. This very sensitive detection mode is used to study the following:
Cell viability assays CellTiterGlo Reporter assays Dual luciferase reporter assay Receptor-ligand-binding BRET-based assays
Another fluorescence-based detection mode uses polarized light to excite the fluorescent molecule. The change of polarization of the emitted light is determined by measuring the emission in the parallel and perpendicular plane relative to the excitation polarization plane. Changes in fluorescence polarization result from differences in molecular weights. Small and light molecules move quickly and depolarize fluorescence emission whereas bigger molecules move slowly and retain fluorescence polarization. This principle allows to study the following:
Competitive binding assays Nucleotide detection to report on enzyme activities Transcreener assays
AlphaScreen (Amplified Luminescent Proximity Homogeneous Assay) technology uses beads that release singlet oxygen when excited with red light (680 nm). Singlet oxygen molecules move up to 200 nm and react with thioxene in a chemiluminescent reaction. Further energy transfers lead either to broad luminescence signals between 520 and 620 nm or to signals with discrete wavelengths. If donor beads (singlet oxygen releasing) and acceptor beads are in close proximity, a luminescent signal is emitted and can be detected by the reader. These beads are usually brought together by antibodies that specifically bind to the same analyte, or that are coupled to molecules that interact with each other. For AlphaScreen detection on a plate reader, excitation at 680 nm is combined with a luminescence readout that is delayed in time, compared to the excitation. AlphaScreen is often used for high throughput applications studying the following:
Protein, cytokine quantification AlphaLISA assays Protein phosphorylations Alpha SureFire assays Protein-protein interactions AlphaScreen assayss
Nephelometry is a technique used to measure the amount of turbidity in a solution caused by the presence of suspended insoluble particles. When directed through a solution containing suspended solid particles, light is transmitted, absorbed, and scattered (reflected off the particles). Nephelometry directly quantifies the intensity of the light scattered by insoluble particles in the sample. A nephelometer is a reader that contains a light source, a detector arranged at a right angle to the light beam, and in between an optical light scattering collector. This principle allows to study the following:
Time-resolved fluorescence (TRF) is a method based on fluorescence that requires excitation of the sample at a specific wavelength and detection of the emitted fluorescence at a different wavelength. Compared to conventional fluorescence intensity, the emission endures for a millisecond instead of a nanosecond timeframe. This is made possible by lanthanides, rare earths with long-lifetime fluorescence characteristics. Readers measure the emission signal with a delay to the excitation, avoiding the detection of background and autofluorescence. TRF is employed for these applications:
Metabolic assays soluble probes for extracellular acidification and oxygen consumption measurements Biomolecule and protein quantification Immunoassay, DELFIA
Time-Resolved FRET (TR-FRET) is a detection technology that combines Time-Resolved Fluorescence (TRF) with Förster´s Resonance Energy Transfer (FRET). TR-FRET is mainly used to analyse binding events and for high-throughput drug screening. FRET describes a transfer of energy between two fluorophores. The transfer depends on the spatial proximity between donor and acceptor and on the overlap between the donor´s emission and the acceptor´s excitation spectrum. TR-FRET kits include HTRF, Lanthascreen, Transcreener and THUNDER, and are employed for these applications:
Binding studies TR-FRET-based assays
Our single-mode plate readers
These microplate readers can measure one detection mode only (typically absorbance, luminescence or fluorescence intensity). These readers are the best choice when it is already clear that the instrument will be used for just one application. Such tasks are typically long-term assays that block the microplate reader for other measurements. Therefore, one detection mode is sufficient. Examples for such studies are microbial growth monitoring which takes one or more days, or thioflavin T experiments which take up to 7 days. A single detection mode reader satisfies your laboratory if you can perform all your assays in a single mode. For instance, with absorbance plate readers you will be able to measure enzyme activities, quantity of DNA and proteins, cell viability and many more. However, you are limited to assays that might have lower sensitivity or specificity than assays employing other detection modes. If you currently plan applications based only on one detection mode but you are not sure what the future brings, look out for plate readers that can later be upgraded to multi-mode instruments.
Our multi-mode plate readers
Instruments capable of reading two or more detection modes are called multi-mode microplate readers. Typically, multi-mode plate readers include absorbance, fluorescence intensity and luminescence, and possibly advanced detection modes. They offer a higher flexibility regarding the assays that are possible to read. Multi-mode readers are recommended whenever many users work on the machine, when your applications change from project to project or, if you already know you need to read assays with different detection modes. Furthermore, a multi-mode plate reader is more cost-effective than multiple dedicated single-mode readers.
Which Plate do I typically use?
6 up to 96 well plates
Image ©Greiner Bio-One GmbH
384 well plates
Image ©Greiner Bio-One GmbH
1536 and 3456 well plates
Image ©Greiner Bio-One GmbH
Which quality features are most important for me?
Microplate readers with the highest sensitivity allow you to read very low signal intensities and to have a better resolution of signals within your assay window. This is most important if your negative and positive control are close together. A highly sensitive reader is mandatory for assays with a very small assay window.
If your needs change during or between projects, a microplate reader that provides numerous possibilities is highly recommended. Consider the capability to switch detection modes, to easily switch between top and bottom reading or to select wavelengths in absorbance, fluorescence and luminescence modes without the need to purchase or install filters. These features are typically provided by monochromator-based multi-mode plate readers. Readers with monochromators enable in addition the acquisition of wavelength scans.
Readers with high detection speed are recommended to measure high density plates (1536 and 3456 well plates), for high-throughput screens, or if a high temporal resolution is needed to resolve quick events (e.g. second messenger signaling).
Which accessories do I need?
Microplate reader accessories extend the capabilities of your instrument. Specific add-on functionalities are required for certain applications like live cell assays, mid-throughput or low volume readings.
What’s my budget?
When it comes to the decision to buy a microplate reader, budget of course plays a role.
The price of a microplate reader depends on the technical equipment and the number of detection modes that the device can measure. The price range of a reader starts at 2.500 Euro/Dollars for a simple filter-based ELISA microplate reader and and could go up to over 150.000 Euro/Dollars for a high-end multi-mode microplate reader with several detection modes and the best technology for highest sensitivity and fastest read times.
But be careful with your choice and don’t consider only your current, but also your future plate reader needs.
Keep an eye on the possibility to upgrade your microplate reader with additional features or detection modes at any time. If you have the chance to upgrade later, you don’t need to buy an additional microplate reader for future applications. This saves not only money and useful space in your lab, but also time that you must bring up to get used to a new plate reader or brand.
Beside the costs for the microplate reader itself, be aware of possible additional hidden costs e.g., fees for servicing, support, software updates and licenses or bundled reagent packages.
Also keep in mind that although filter-based readers are usually cheaper than monochromator-based instruments, you need to purchase different filters for different wavelengths. Be sure to factor in those costs as well.
Why to choose a BMG LABTECH microplate reader?
BMG LABTECH is specialized in producing microplate readers only and brings 30 years of full expertise in microplate reading technology. This knowledge gets visible in the results that our instruments deliver - the only factor that counts in your lab! BMG LABTECH users can trust to receive best results in sensitivity, speed and flexibility. Moreover, our plate readers are developed to provide optimum performance for years. Our instruments are developed, produced and tested in Germany and are built to be extremely robust and reliable.
One quality seal is our product ranking on the established scientific platform "Select Science", where our customers gave us 4.7 out of 5.0 stars. Don't miss to read what our users have to say about our microplate readers.
Buy only what you need
Due to their modularity, all our plate readers can be equipped with different detection modes and cover a multitude of applications. Additional features can be upgraded at any time. This gives you the chance to keep your options open even if you don’t use the full scope of your microplate reader right at the bat.
All-round service and support
At BMG LABTECH we strive to provide you with the very best customer service. If you need customer support, we are only a phone call or email away. During business hours, you immediately speak live to a person who is happy to assist. There is no automated phone system or waiting in a queue, our scientists, engineers and technicians are always there to help.
Multi-user software package
All our instruments come with a multi-user software package that can be installed on as many computers as users requires, without the need to purchase licenses. Software updates for our microplate readers are of no charge within the first 12 month after purchase.