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必威体育登录手机Introducing an automated neurite analysis module for Agilent BioTek imaging systems, with iPSC-derived and primary neuron culture model evaluations.
必威体育登录手机This study shows the ability of Agilent BioTek instrumentation to quantitate changes in IL-2 secretion in Jurkat cells using a silver-stain ELISPOT assay format.
In this application note, the nuclear translocation of the protein RelA is quantitated in macrophages using image-based analysis.
This study describes the use of the Cytation 5 cell imaging multimode reader to rapidly image and analyze a number of different lipid stained tissue culture cells.
必威体育登录手机This application note examines the production of lipid droplets in HepG2 cells exposed to palmitic and oleic acids using Agilent BioTek instrumentation.
This application note describes the use of the Lionheart FX automated microscope to rapidly image and analyze perfused tissue culture cells.
必威体育登录手机This application note describes the capabilities of the Agilent BioTek Gen5 software to analyze mitochondrial membrane potential by object spot counting.
This application note describes the use of immune-fluorescent stained PC-3 cells as a means to calculate cell cycle time.
必威体育登录手机This application note describes the automation of the non-alcoholic fatty liver disease model assay workflow using Agilent BioTek instrumentation.
This study describes the use of automated object-based spot counting to quantitatively assess the effects of starvation and rapamycin on cellular autophagy.
This application note presents data using PrimeSurface ULA plates to develop spheroid assays for brightfield and fluorescence imaging.
This application note describes the use of an automated tool to create consistent scratch wounds in cell monolayers formed on the bottom of a microplate well.
In this study, a common IVD application was used as a model to demonstrate image analysis of direct immunofluorescence.
This application note demonstrates the benefits of a live cell imaging-based approach to measuring calcium-dependent Fluo-4 AM fluorescence.
This application note describes an imaging-based approach to measure changes in cAMP levels over time in live cells.
This application note demonstrates high throughput screening and analysis of zebrafish embryos treated with several developmental toxins.
This study describes the use of the Lionheart FX and Cytation automated imagers in providing a powerful and convenient system to characterize Ca2+ flux using R-GECO.
This application note demonstrates that zebrafish treated with ethanol have a dose-dependent increase in apoptotic cell death.
This application note describes a rapid, reproducible method for imaging and analyzing viability of fluorescently stained soil bacilli.
This application note describes an automated microscopy and analysis protocol as an alternative method for AFB scoring.