Cellometer Application GalleryCellometer instruments are used for a wide variety of cell types and applications from basic cell counting and viability to fluorescence cell-based assays. Browse through our application gallery to see how Cellometer can be used in your lab. For more applications, please visit our user publication page.
When should you use trypan blue and when should you use acridine orange/propidium iodide to measure cell viability? »
Automatically measure the cell cycle of mammalian cells. Generated cell cycle histogram allows for easy data analysis and presentation. »
Analyze fresh and processed blood and bone marrow samples without lysing: no interference from RBCs. »
Automatically measure live cell concentration and viability without lysing red blood cells for consistent results from patient samples. Other cells include splenocytes and bone marrow. »
Analyze autophagy activity in living cells using CytoID® Green dye and GFP-labeled LC3 marker. Fluorescence histograms are used to measure mean fluorescence intensity of live cells, and then used to determine the autophagy activity factors in the population. »
Automatically measure live hepatocyte concentration and viability using dual fluorescent nuclear stains, for human, rat, mouse and horse. »
Performing cell size measurement assay and using cell size to count cells within preset cell size parameters. For adipocytes, stem cells, Sf9 cells, dendritic cells, and others. »
Rapidly identify fluorescence positive cells from a sample, analyze individual cell fluorescence intensity, calculate cell concentration, size and determine the GFP transfection automatically. »
Live yeast cell concentration and viability are measured automatically based on the membrane permeability of the fluorescent dye Oxonol. Multiple strains of yeast with viability ranging from 88 to 5% were measured. »
Automatically detect and analyze Caspase3 and 8, JC-1, and Annexin V apoptotic events using the Cellometer image cytometery. »
Cell viability is performed using various fluorescent membrane exclusion dyes, such as PI, EB, 7AAD, and others. This assay is performed by enumerating cells in captured bright-field and fluorescent images. And Necrotic cells are detected using propidium iodide. »
Automatically measure live cell concentration and viability for stem cells, such as human and mouse ES cells, mesenchymal, cardiac, induced pluripotent stem cells. Multiple viability stains, such as trypan blue, propidium iodide are used to identify dead cells. For samples with a lot of debris, dual fluorescent nuclear stains are used for live and dead cells. »
Automatically quantify cell viability and concentration for a variety of immunologically relevant samples such as: bone marrow, cord blood, slpenocytes, lymphocytes, isolated mononuclear cells, tumor digests, murine samples, and others. »
Automatically measure nucleated cell concentration without lysing red blood cells using nuclear staining dyes (AO), for human and mouse blood. »
Automatically measure cell size of freshly isolated adipocytes and plot size histogram. DNA staining fluorescence dyes are used to identify cells from lipid droplets. »
Automatically measure mouse and human platelet concentration using brightfield only method. »
Automatically measure live cell concentration, viability for baculovirus infected insect cells. Cell size histogram live cell concentration and viability are generated within less than 60 seconds using 20 µl sample. »
Online and on site Cellometer demos and new user training are available.
Demonstrations, webinars, Cellometer features, assay principles and much more.
Our cell image gallery with hundreds of cell types...
A series of mini presentations.
View recent Cellometer product references from peer-reviewed publications.