Cell health

The ApoLive-Glo Multiplex Assay measures both the number of viable cells as a marker of cytotoxicity and caspase activation as a marker of apoptosis within a single assay well to determine the mechanism of cell death

The ApoTox-Glo Triplex Assay combines three assay chemistries to easily assess viability, cytotoxicity and apoptosis events in the same cell-based assay well.

The BacTiter-Glo Microbial Cell Viability Assay is a homogeneous method for determining the number of viable microbial cells in culture based on quantitation of the ATP present

Z-VAD-FMK is a cell-permeant pan caspase inhibitor.

CellTiter 96(R) AQueous MTS Reagent Powder is a novel tetrazolium compound for use in colorimetric assays to determine the number of viable cells in proliferation, cytotoxicity or chemosensitivity assays.

Homogeneous, colorimetric cell viability assay; requires mixing of MTS and PMS components prior to assay, then a 1- to 4-hour incubation. Standalone MTS powder for applications where optimization of assay for specific cell types or conditions is desired.

Colorimetric cell viability assay (MTT). Solubilization step is required.

Homogeneous, fluorometric cell viability assay (resazurin). Requires a 1- to 4-hour incubation

The CellTiter-Glo 2.0 Assay provides a homogeneous method of determining the number of viable cells in culture by quantitating the amount of ATP present, which indicates the presence of metabolically active cells.

The CellTiter-Glo 3D Cell Viability Assay is a homogeneous method to determine the number of viable cells in 3D cell culture based on quantitation of the ATP present, which is a marker for the presence of metabolically active cells

A Luminescent Assay to Determine the Number of Viable Cells in Culture. Designed for use with multiwell formats, making it ideal for automated HTS, cell proliferation and cytotoxicity assays. The homogeneous assay procedure involves adding the single reagent (CellTiter-Glo® Reagent) directly to cells cultured in serum-supplemented medium.

The CellTiter-Glo One Solution Assay is a homogeneous method of determining the number of viable cells in culture based on quantitation of the ATP present, which indicates the presence of metabolically active cells

The CellTox Green Cytotoxicity Assay measures changes in membrane integrity that occur as a result of cell death. The assay is intended to assess cytotoxicity in cell culture after experimental manipulation.

The CytoTox-Fluor Cytotoxicity Assay is a single-reagent-addition, homogeneous, fluorescent assay that measures the relative number of dead cells in cell populations

The CytoTox-Glo Assay is a luminescent cytotoxicity assay that measures the relative number of dead cells in a population

A fast homogeneous, fluorometric method for estimating the number of non-viable cells present in multiwell plates. Based on detection of LDH release, an indicator of cytotoxicity

A modified TUNEL Assay designed for simple, rapid detection of apoptotic cells in situ at the single-cell level. Measures nuclear DNA fragmentation.

The FastMitophagy Detection Kit is specifically designed for mitophagy detection in mammalian cells. Mitophagy is the selective degradation of defective mitochondria by autophagy following DNA damage or oxidative stress. It serves as a specific elimination system by sequestering dysfunctional mitochondria into autophagosomes, fusing the phagosome to lysosomes, and degrading them by digestion. Since its first observation in 1962, mitophagy has attracted intense research for cell homeostasis and development in mammalian cells.

Simple, More Sensitive LDH Assay Method to Determine Cytotoxicity