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Hybrid multimode microplate reader with proprietary Hybrid Technology
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(IVD) Features patented Hybrid Technology
This document is an information guide and checklist prepared for you that outlines the supplies, space, and utility requirements for the system set up in your lab.
This application note describes how the Agilent BioTek 406 FX washer dispenser increases a laboratory’s efficiency and productivity by automating the liquid handling steps of the CellTiter-GLO assay.
This application note presents a novel HTRF cell-based assay that quantifies endogenous phosphorylated retinoblastoma protein.
Biotek Synergy neo2 xenon flash lamp light dose
Biotek Synergy neo2 xenon flash lamp light dose
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Hi All, Is there a way to measure or estimate light dose (e.g. in units of mJ/cm^2 per flash) when reading fluorescence at particular wavelength/bandwidth? And what the spot size is when reading 96-well plate? The idea is to use the plate reader to photoconvert a compound (at 590 nm) and then use it immediately to measure the response (fluorescence, absorbance). Thank you!
Biotek Synergy HT microplate reader
Biotek Synergy HT microplate reader
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I am trying to run the kinetics of catalase decay against H2O2 using 240 nm absorbance. I am using Biotek Synergy HT microplate reader and Gen5 software. I need the kinetics every second or 15 second at maximum for 2 minutes. I am not able to adjust the time to get reading every 15 second.
Setting Gain for Measuring Fluorescence Using Biotek Synergy H1 Microplate Reader
Setting Gain for Measuring Fluorescence Using Biotek Synergy H1 Microplate Reader
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I am using a Biotek Synergy H1 microplate reader and the Gen5 software version 3.12.8. I have been trying to measure fluorescence using the machine, but I am having trouble setting the gain.
Sudden Spikes or Drops in A340 Kinetic Reads on Agilent BioTek Microplate Readers
Sudden Spikes or Drops in A340 Kinetic Reads on Agilent BioTek Microplate Readers
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I’m experiencing an intermittent issue with several Agilent BioTek microplate readers (Epoch, Epoch 2, and Synergy H1) running GEN5 versions 3.14. During kinetic absorbance measurements at 340 nm in 96 well plates, one or a few wells will occasionally show a large, sudden drop—or sometimes a sharp increase—in absorbance between time points.
This application note describes the use of the Agilent BioTek Synergy Neo2 hybrid multimode reader to rapidly determine IgG concentrations.
This technical overview describes the Gen5 parameters required to establish a standard curve and perform a DNA quantification with the Qubit dsDNA BR assay reagent.
This study shows the ability to record excitation and emission spectra for fluorescent probes using the monochromator-based detection system of a microplate reader.
This technical overview describes the use of angled dispense tips for assay optimization.
This application note describes the use of the Synergy H1 reader along with UV-capable fluorescence polarizers to investigate mass changes of proteins in solution.
This application note demonstrates the ability of the Agilent BioTek Synergy Neo2 in conjunction with PhosphoSens detection technology to quantify kinase activity.
This application note illustrates the capabilities of the Agilent BioTek Synergy Neo2 when performing a new BRET technology, NanoBRET in a cell-based, HTS format.
In this application note, specialized NanoBit CX3CR1/ ARRB2 cells are used to demonstrate the GPCR: ß-arrestin2 recruitment assay.
This application note shows kinetic degradation profiling of IMiD molecular glues and their targets using Agilent BioTek BioSpa 8 and Synergy Neo2 instrumentation.
This application note investigates the performance of several luciferase variants and assay formats across a range of compatible Agilent BioTek microplate readers.
This application note examines the drug-target residence time of various CXCR4 inhibitors using a direct, homogeneous ligand binding assay.
This application note describes the rapid semi-automated determination of CMC values for surfactants in 384-well microplates using fluorescence polarization.
This application note describes two homogeneous HTRF assay formats to assess the small molecule inhibitor capabilities of methyltransferase and demethylase enzymes.
This application note investigates the performance of a dual luciferase assay using two luciferases with spectrally resolvable light emissions.
This application note describes a cell-based method using AlphaScreen SureFire technology to determine endogeneous cellular kinase activity.