Abstract
An enzyme immunoassay, in which an enzyme (e.g., alkaline phosphatase, ALP) is conjugated with an antibody, is a precise and simple protein detection method. Precise measurements of enzymes at low concentrations allow for ultrasensitive protein detection. The application of a phosphorylated substrate to ALP, followed by using a dephosphorylated substrate in thionicotinamide-adenine dinucleotide cycling, provides a simple and precise quantification of ALP. We describe a protocol for detecting ALP at the zeptomole level using a simple colorimetric method.
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CITATION STYLE
Iha, K., Kyosei, Y., Namba, M., Makioka, D., Yamura, S., Watabe, S., … Ito, E. (2021). Zeptomole Detection of an Enzyme by a Simple Colorimetric Method Kanako. Analytical Sciences, 37(10), 1469–1472. https://doi.org/10.2116/analsci.21N009
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