Luminescent assays for measuring cytochrome P450 activity, including systems with suitable for cell-based assays and DMSO-tolerant substrates.
The UGT-Glo™ Assay provides a luminescent method for measuring UDP glucuronosyltransferase activity. Complete assay systems are available for UGT1A1 and UGT2B7.
A luminescence-based assay that detects the effects of compounds on recombinant human Pgp in a cell membrane fraction.
A homogeneous luminescent method for measuring MAO activity from recombinant and native sources, as well as the effects of test compounds on MAO activities.
A single-reagent fluorescent assay with a flexible protocol to perform kinetic or endpoint cytotoxicity analysis after extended exposure.
Determine Mechanism of Cell DeathThe Apo-ONE® Homogeneous Caspase-3/7 Assay is a fast, sensitive, fluorescent apoptosis detection system featuring a homogeneous format.
The Caspase-Glo® Assays monitor toxic effects of compounds at high-throughput capacities, or one sample at a time, in as little as 15 minutes.
Monitor cell viability out to 72 hours in the same well. No cell washing, media removal or further additions required. Add at plating, during treatment or at the end of treatment.
Accurate cytotoxicity determination validated for 3D microtissue cultures. Easy assay implementation. Simple, 30-minute protocol.
Directly measure the key energy metabolite ATP, resulting in sensitive quantitation of the number of healthy cells in culture using this simple assay.
Control variability by quantifying the number of live and dead cells within a single well.
A single-reagent fluorescent assay with a flexible protocol to perform kinetic or endpoint cytotoxicity analysis after extended exposure.
measures 3 key independent biomarkers for viability, cytotoxicity and apoptosis in the same sample well.
Control variability by quantifying the number of live and dead cells within a single well.
A single-reagent-addition, homogeneous, fluorescent assay that measures dead-cell protease activity released from cells that have lost membrane integrity.
A rapid, fluorescent measure of the release of LDH from cells with damaged membranes. Can be used to measure released LDH in plate wells containing a mix of viable and damaged cells.
A luminescent cytotoxicity assay that measures the relative number of dead cells in cell populations.
A homogeneous bioluminescent assay that quantifies NADH and NADPH and does not discriminate between them. The oxidized forms, NAD+ and NADP+, are not detected and do not interfere with quantitation.
A homogeneous, bioluminescent assay for directly detecting total oxidized and reduced nicotinamide adenine dinucleotides (NAD+and NADH, respectively) and determining their ratio in biological samples.
A homogeneous, bioluminescent assay for directly detecting total oxidized and reduced nicotinamide adenine dinucleotide phosphates (NADP+ and NADPH, respectively) and determining their ratio in biological samples.
A homogenous, multiwell plate-based assay to selectively detect caspase-1 activity as a biomarker for inflammasome activation. This assay is a faster, simpler alternative to Western blot and ELISA assays for detecting cleaved caspase-1 and interleukin 1β
A multiplexed, cell-based assay to monitor mitochondrial health. Measures ATP and a membrane integrity biomarker to distinguish mito-toxic mechanisms from other cytotoxic events.
A cell-based multiplexed method that measures ATP as an indicator of mitochondrial function and uses a membrane integrity biomarker to distinguish primary mitochondrial dysfunction from secondary cytotoxic events.
A rapid, sensitive bioluminescent assay to identify conditions or test compounds that alter ROS levels. Eliminates false-hits associated with HRP methods.
GSH-Glo™ Glutathione Assay
Detects and quantifies glutathione in cells or in a variety of biological samples, providing a sensitive alternative to colorimetric and fluorescent methods. Suitable for HTS.
GSH/GSSG-Glo™ Assay
Detects and quantitates total glutathione and GSSG to allow calculation of ratio of reduced (GSH) to oxidized glutathione (GSSG).
State-of-the-art luciferase reporter technology integrated into a cell line allows rapid development of reporter assays based on the pathway of interest regulating the luciferase gene. Cell lines containing CRE, NFAT, NF-κB and GAL4UAS response elements are available.
Reporter Vectors for Toxicity Pathway Analysis
These vectors report the activity of a variety of signaling pathways using the luc2 firefly luciferase gene. Each vector contains a response elements upstream of a minimal promoter (minP). Choose the appropriate vector for your signaling pathway of interest.
Custom Materials for Toxicity Pathway Analysis
We offer a number of specific Toxicity Pathway Reporters and Cell Lines, which are available for sale by quote.
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