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Cell Counting and Image Cytometry

Viability and Cell Health

Section
Celigo Applications
Celigo Applications
Cell Counting Method Selection
Cell Counting and Image Cytometry FAQs
Cell-based Assays for Bioprocessing
Cell-based Assays for Gene Therapy Development
Cellometer Applications
Modern Virology Assays
Sub Section
Celigo Fluorescent Assays
3D Cell Models
Assays for Virology Research
Brightfield Applications
Celigo Cell Counting Applications
Celigo Fluorescent Assays
Celigo Image Cytometer Direct Cell Counting Assays for Immunotherapy
Cell Line Development
Migration and Invasion Assays
iPSC Reprogramming
Topic
Viability and Cell Health
Celigo Fluorescent Assays - Apoptosis
Celigo Fluorescent Assays - Wound Healing
Cell Cycle
Co-culture
Internalization and Phagocytosis
Surface Proteins and Antibodies
Transfection and Transduction
Viability and Cell Health

Analysis of cell health using the Celigo™ image cytometer has several advantages:

  1. Easy-to-use interface to identify cell health
  2. Rapid scanning and analysis (scan and analyze a 96-well plate using 3 fluorescent channels in <12 min)
  3. Works in multi-well plate formats (1536-well to 6-well)
  4. Advanced flow cytometry-like gating

Viability introduction

Quick assessment of cell health is performed using the Celigo image cytometer with its easy-to-use applications that allow the simple and rapid analysis of cell viability and apoptosis in many diverse cell types. The Cell Viability application uses Calcein AM, propidium iodide and Hoechst to identify and count live, dead and total cell numbers, respectively. Similarly, the Phosphatidylserine (PS) Externalization application measures apoptosis by quantifying annexin V, propidium iodide and Hoechst to report apoptotic, dead and total cell counts, respectively.

Cell viability application on the Celigo image cytometer

Celigo cell viability

Image of heLa cells & Concentration response curve

Briefly, cells are simultaneously stained with a mixture of Calcein AM, propidium iodide and Hoechst 33342 for staining of live, dead and all cells, respectively. Images are acquired and analyzed using the Celigo software. Markers are identified in each fluorescent channel and for each well of a microtiter plate. Live and dead cell counts as well as the percentage of live and dead cells are automatically reported.

Fluorescence live dead staining

Live / Dead

Live / Total

Live / Total


For research use only. Not for use in diagnostic procedures.

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