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.
Colorimetric assay for the determination of cell membrane integrity based on detection of LDH release, an indicator of cytotoxicity. Sample transfer steps are required.
The NAD/NADH-Glo™ Assay is a bioluminescent, homogeneous single-reagent-addition assay for detecting total oxidized and reduced nicotinamide adenine dinucleotides and determining their ratio in biological samples or in defined enzyme reactions.
The RealTime-Glo™ MT Cell Viability Assay is a non-lytic, homogeneous, bioluminescent method to determine in real time the number of viable cells in culture by measuring the reducing potential of cells and thus metabolism (MT).
The CellTiter-Fluor Cell Viability Assay is a non-lytic, single-reagent-addition fluorescence assay that measures the relative number of viable cells in a population.
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.
Quantifies LDH activity in variety of biological samples such as serum or plasma, cells, culture medium and fermentation, etc. The assay is quick, convenient, and sensitive. The kit can detect 1 to 100 mU/mL of LDH directly in samples.
