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1st-generation ATP tests are derived from hygiene monitoring uses where samples are relatively free of interferences. 2nd-generation tests are specifically designed for water, wastewater and industrial applications where, for the most part, samples contain a variety of components that can interfere with the ATP assay.
A viability assay is an assay that is created to determine the ability of organs, cells or tissues to maintain or recover a state of survival. [2] Viability can be distinguished from the all-or-nothing states of life and death by the use of a quantifiable index that ranges between the integers of 0 and 1 or, if more easily understood, the range ...
This allows luciferase to detect the efflux of ATP from the cell and will effectively display the real-time release of ATP through bioluminescence. [22] Luciferase can additionally be made more sensitive for ATP detection by increasing the luminescence intensity by changing certain amino acid residues in the sequence of the protein. [23]
The Microtox Model 500 is a laboratory-based photometer that measures acute toxicity.This analyser is a temperature-controlled, self-calibrating biosensor measuring system that uses the bioluminescence of Allivibrio fischeri to determine the toxicity of contaminated water, or elutriates of contaminated soils and sediments.
The ATPase assay is a membrane assay that indirectly measures the activity of efflux transporters. ATP Binding Cassette or efflux transporters mediate the transport of substrates across cell membranes against a concentration gradient .
Many of the detection modes (absorbance, fluorescence intensity, luminescence, time-resolved fluorescence, and fluorescence polarization) are available stand-alone in dedicated plate readers, but are very often found today combined into one instrument (multi-mode plate reader).
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