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    Agilent BioTek Synergy H1 Multimode Reader

    Agilent BioTek Synergy H1 multimode reader is a configurable multimode microplate reader, with monochromator-based optics for flexibility, filter-based optics for sensitivity, or both. Hybrid Technology offers application versatility and excellent performance in a modular platform to expand as your laboratory’s needs change.

    Not available from Chemetrix in Kenya.

    Features

    • Hybrid plate reader provides flexibility and performance with a combination of monochromator and filter optics for any microplate assay and flexible detection capabilities.
    • Upgradable, modular design allows for added detection modes, gas control, and dual reagent injectors as your laboratory workflows evolve.
    • Variable bandwidth settings range between 9 and 50 nm, in 1 nm increments for either increased sensitivity or increased specificity.
    • Automated Z-focus provides the best performance for all plate types and at low volumes, adjusting reading height to deliver high-performance measurements and high-quality data.
    • Extended dynamic range enables signal detection across a 7 log measurement range, delivering high sensitivity in low-end measurements and preventing saturated signals in high-end measurements.
    • Environmental controls and robust shaking profiles enable consistent data in live cell assay workflows, including temperature control to 70 °C and CO2/O2 control.
    • Dual syringe injectors with specialized tips eliminate the need for regular tubing replacement, and two tip types offer flexible use with straight tips for vigorous mixing and rapid inject/read assays or angled tips that do not disturb cell layers.
    • Microvolume analysis with Take3 plate measures up to 16 or 48 samples in one run, saving time compared to single-sample devices.

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    Applications

    • ELISA
    • Luciferase Reporter assays
    • Nucleic acid and protein quantification
    • Microbial growth assays
    • TR-FRET
    • Fluorescence polarization
    • BRET
    • Enzyme kinetics
    • Protein aggregation
    • Cell-based assays
    • Metabolic activity
    • ROS

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