logo
AAT Bioquest

Multiplex Apoptosis and Necrosis

Apoptosis is an active, programmed process of autonomous cellular dismantling that avoids eliciting inflammation. In apoptosis, phosphatidylserine (PS) is transferred to the outer leaflet of the plasma membrane. As a universal indicator of the initial/intermediate stages of cell apoptosis, the appearance of phosphatidylserine on the cell surface can be detected before morphological changes are observed.

Necrosis is characterized as a passive, accidental cell death resulting from environmental perturbations with uncontrolled release of inflammatory cellular contents. Loss of plasma membrane integrity represents a straightforward approach to demonstrate late stage apoptosis and necrosis.

AAT Bioquest offers Cell Meter™ Apoptotic and Necrotic Detection Kits as a set of tools for monitoring cell viability. Our Cell Meter™ detection kits are optimized to simultaneously detect cell apoptosis, necrosis and healthy cells with a flow cytometer or fluorescence microscope. The phosphatidylserine (PS) sensor used in Kit 22843 has deep red fluorescence (Ex/Em = 630/660 nm) upon binding to membrane PS. Membrane-impermeable Nuclear Green™ DCS1 (Ex/Em = 490/525 nm) is used to label the nucleus while CytoCalcein™ Violet 450 (Ex/Em = 405/450 nm) is provided for labeling live cell cytoplasm.

Key Features of Cell Meter™ Detection Kits:

  • Multiplexing capability, triple colors for the simultaneous detection of multiple cellular events.
  • Robust, a mix and read format.
  • Convenient, compatible with common filter sets.

Non-induced control cells and Triple staining of staurosporine-induced cells.

The detection of binding activity of Apopxin™ Deep Red to phosphatidylserine in Jurkat cells. The fluorescence images demonstrated Jurkat cells that are live (blue, stained by CytoCalcein™ Violet 450), apoptotic (red, stained by Apopxin™ Deep Red), and necrotic (green, indicated by Nuclear Green™ DCS1staining). The cells were induced by 1µM staurosporine for 3 hours. The fluorescence images of the cells were taken with Olympus fluorescence microscope through the Violet, Cy5 and FITC channels respectively. Individual images were taken from each channel for the same cell population. The images were merged as shown above. A: Non-induced control cells; B: Triple staining of staurosporine-induced cells.

 

Table 1. Cell Meter™ Assay Kits for Detecting Apoptosis and Necrosis

Cat No.
Product Name
Ex (nm)
Em (nm)
Unit Size
22840Cell Meter™ Apoptotic and Necrotic Multiplexing Detection Kit I *Triple Fluorescence Colors* 100 Tests
22843Cell Meter™ Apoptotic and Necrotic Multiplexing Detection Kit II *Triple Fluorescence Colors* 100 Tests
22811Cell Meter™ Nuclear Apoptosis Assay Kit *Green Fluorescence Optimized for Flow Cytometry*503526100 Tests
22844Cell Meter™ Live Cell TUNEL Apoptosis Assay Kit *Red Fluorescence*55657950 Tests
13433Z-DEVD-ProRed™ 6205346191 mg