
BioTek Cytation 5 Cell Imaging Multimode Reader
BioTek Cytation 5 Cell Imaging Multimode Reader
The multimode detection modules include filter- and monochromator-based fluorescence detection, luminescence, and UV-Vis absorbance detection. Gen5 IVD software provides features for IVD compliance requirements.
- Clinical Imaging Multimode Readers
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Product Details
- Fully validated for IVD use
- Gen5 IVD software provides features for IVD compliance requirements
- Modular, upgradable imaging modes, plus multimode detection enables a range of cell-based assays and applications beyond a standard microplate reader
- Increase productivity with a system that is ready for any assay, with a combination of hybrid plate reader and advanced microscopy mode
- Fully automated microscopy tasks, from slide scanning to time lapse live cell assays, and flexible hardware to increase productivity and reduce manual labor
- A combination of monochromator and filter optics delivers flexibility and performance to microplate assays. A choice of optics allows you to read microplates in a wide range of applications
- BioTek Gen5 software enables walkaway automation for your image process and analysis workflows and data analysis tasks
- Variable bandwidth quad monochromator optics enhance assay performance including increased sensitivity and lower limits of detection
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Monochromator Detection Modes |
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Hybrid plate reader: Flexibility and performance
With its patented combination of monochromator and filter optics, Cytation 5 is an advanced plate reader that delivers both the flexibility and performance you need for any microplate assay in your lab. Monochromator: variable bandwidth, absorbance, fluorescence, luminescence Filters: fluorescence polarization, time-resolved fluorescence, Alpha laser.
Learn MoreVariable bandwidth for sensitivity and specificity
The plate reader optics of Cytation uses a quad monochromator design with variable bandwidth. The bandwidth can be set anywhere between 9 and 50 nm in 1 nm increment. Large bandwidth settings (1) provide increased sensitivity and lower limits of detection. Small bandwidth settings (2) provide increased specificity when multiple signals are present, which reduces signal crosstalk and enhances assay performance.
Learn MorePeltier cooling for environmental stability
The Peltier Cooling Module promotes a rapid interior cool down after incubated processes, allowing efficient switching between multiple applications. For temperature sensitive assays run at room temperature, the Cooling Module maintains temperature, allowing < 1 °C rise regardless of internal or external fluctuation.
Learn MorePatented laser autofocus
Laser autofocus and image-based (or software-based) autofocus are two methods of autofocus widely used in microscopy.
Learn MoreTime-resolved fluorescence
Time-resolved fluorescence (TRF) measurement is very similar to fluorescence intensity (FI) measurement. The only difference is the timing of the excitation / measurement process.
Learn MoreAlpha detection
AlphaScreen is a bead-based assay technology used to study biomolecular interactions in a microplate format. The acronym 'Alpha' stands for amplified luminescent proximity homogeneous assay. This platform provides a nonradioactive, homogeneous assay that has low background and high signal to background ratios.
Learn MoreAbsorbance
Absorbance refers to the ability of a substance to absorb light of a specific wavelength. In a microplate reader designed to measure absorbance, a light source illuminates the sample using a specific wavelength, selected by an optical filter or a monochromator.
Learn MoreFluorescence polarization
Fluorescence polarization (FP) measurements are made using an optical system that includes polarizing filters in the light path. Samples in the microplate are excited using polarized light. Depending on the mobility of the fluorescent molecules found in the wells, the light emitted will either be polarized or not.
Learn MoreTR-FRET
Time-resolved fluorescence energy transfer (TR-FRET) works on the principles that when suitable pairs of fluorophores are in close proximity of one another, excitation of a lanthanide donor fluorophore results in energy transfer to an acceptor fluorophore.
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