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Catalog Number | Measurement Technology | Reading Options | No. of Dispensers |
---|---|---|---|
VLBL00GD0 | Absorbance, Fluorescence Intensity, Luminescence | Top and Bottom | None |
VL0000D0 | Absorbance, Fluorescence Intensity | Top | None |
VL0L00D0 | Absorbance, Fluorescence Intensity, Luminescence | Top | None |
VL0L0TD0 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence | Top | None |
VLBL00GD1 | Absorbance, Fluorescence Intensity, Luminescence | Top and Bottom | 1 |
VLB000D0 | Absorbance, Fluorescence Intensity | Top and Bottom | None |
VLBL00GD2 | Absorbance, Fluorescence Intensity, Luminescence | Top and Bottom | 2 |
VLBL00D0 | Absorbance, Fluorescence Intensity, Luminescence | Top and Bottom | None |
VLBL0TGD0 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence | Top and Bottom | None |
VLBL0TGD1 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence | Top and Bottom | 1 |
VLBLATD0 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence, AlphaScreen | Top and Bottom | None |
VLBL0TGD2 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence | Top and Bottom | 2 |
VLBLATGD0 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence, AlphaScreen | Top and Bottom | None |
VLBLATGD1 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence, AlphaScreen | Top and Bottom | 1 |
VLBLATGD2 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence, AlphaScreen | Top and Bottom | 2 |
VLBL00D1 | Absorbance, Fluorescence Intensity, Luminescence | Top and Bottom | 1 |
VLBL0TD1 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence | Top and Bottom | 1 |
VLBLATD1 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence, AlphaScreen | Top and Bottom | 1 |
VLBL00D2 | Absorbance, Fluorescence Intensity, Luminescence | Top and Bottom | 2 |
VLBL0TD2 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence | Top and Bottom | 2 |
VLBLATD2 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence, AlphaScreen | Top and Bottom | 2 |
VLBL0TD0 | Absorbance, Fluorescence Intensity, Luminescence, Time-resolved Fluorescence | Top and Bottom | None |
Designed for bioscience researchers with a wide variety of needs, the Thermo Scientific™ Varioskan™ LUX multimode microplate reader comes equipped with a flexible range of measurement technologies including Absorbance, Fluorescence Intensity, Luminescence, AlphaScreen, and Time-Resolved Fluorescence. The instrument simplifies measurement setup with the automatic dynamic range selection, and its smart safety controls ease workflow and help avoid experimental errors. Varioskan LUX raises the bar for reliability and ease, with technology that works in researchers' best interest.
The Varioskan LUX multimode reader has received HTRF™ certification from Cisbio Bioassays and DLReady™ validation from Promega Corporation.
The Varioskan LUX is a modular, upgradable instrument that provides excellent usability across a variety of applications.
Varioskan LUX is paired with the powerful and intuitive SkanIt Software, providing excellent usability and flexibility.
The Varioskan LUX is modular and upgradeable, so you can build the system that best suits your needs. For more information, contact a sales representative.
Fast and reliable results, even for the most challenging of applications.
Download our brochure ›
How can built-in smart safety controls help avoid errors in microplate assay experiments?
How will automatic dynamic range selection ease workflow and improve the outcome of my microplate assays?
Thermo Scientific SkanIt Software comes free with your microplate reader purchase and can be installed on as many computers as you like. This easy-to-use program is so intuitive, it requires little-to-no training. SkanIt Software has features that help boost productivity and prevent common errors in the lab.
Learn more ›
Power off the Varioskan LUX instrument, open the sliding door, and then press both springs outward (1) to unlock the bottom of the front panel. Tilt the bottom of the panel outwards slightly and lift up to remove.
Look inside the instrument to locate the tray (3). Gently slide the tray to the left and then towards you to access the plate. Check for jams and make sure that the correct holder is installed. When finished, push the tray back into the instrument (exact position doesn’t matter as long as it is completely inside) and reinstall the front panel.
Note: Remove the bottom front cover on the instrument, in order to access the plate carrier, and manually pull out the plate. Do not attempt to grab the plate back through the plate door, otherwise it can cause alignment issues that will require a repair.
Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.
We recommend transporting the Varioskan LUX Multimode Microplate Reader in the original packaging it was delivered in, with proper padding in the box, and after securing the tray holder transport lock on the instrument. See page 84 of the user manual for instructions to refit the transport lock of the tray holder.
Note: We also offer a service to move the instrument. Please reach out to serviceproducts@thermofisher.com.
All of the DNA instruments offered by Thermo Fisher Scientific are of excellent quality. To find the right instrument to quantify DNA or RNA in your lab, explore the detailed comparison of UV-Vis spectrophotometers and fluorometers. Things like sensitivity, throughput and budget may be initial considerations when selecting a DNA quantification instrument. You may also consider whether you need target specificity, sample purity information, RNA quality information, or broad dynamic range.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Quantification Support Center.
UV and fluorescence technologies work differently to quantify DNA. UV quantification relies on the intrinsic absorptivity of DNA and RNA molecules, while fluorescence quantification uses dyes that specifically bind to your molecule of choice. With UV technology, quantification isn't as sensitive, but it has a broader dynamic range and also gives data about sample purity‒plus it is faster because there is no reagent prep. With fluorescence technology you get higher sensitivity and molecule-specific data, but it has lower dynamic range and reagent prep is required. The technology you need will depend on what features are important for your lab and experimentation.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Quantification Support Center.
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