Automated Analysis of Primary Cells
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 live hepatocyte concentration and viability using dual fluorescent nuclear stains, for human, rat, mouse and horse.
Automatically measure live cell concentration and viability for stem cells. Multiple viability stains can be used to identify dead cells. For samples with a lot of debris, dual fluorescent nuclear stains are used for live and dead cells.
A head-to-head comparison of viability determined by TB and AO/PI.
Measure the concentration and viability of nucleated cells in a primary SVF sample.