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An assay (analysis) is never an isolated process, as it must be accompanied with pre- and post-analytic procedures. Both the communication order (the request to perform an assay plus related information) and the handling of the specimen itself (the collecting, documenting, transporting, and processing done before beginning the assay) are pre-analytic steps.
On the wet basis the value is the ratio of the weight of water to the total weight of the solution (1 / 5 = 20% in the example), so the moisture content is always below 100% (in the previous examples the moisture content was specified on this "moisture content wet basis"). For the moisture content dry basis the ratio of the weight of the water ...
If the measured response is binary, the assay is quantal; if not, it is quantitative. [3] A bioassay may be used to detect biological hazards or to give an assessment of the quality of a mixture. [4] A bioassay is often used to monitor water quality as well as wastewater discharges and its impact on the surroundings. [5]
A mobility shift assay is electrophoretic separation of a protein–DNA or protein–RNA mixture on a polyacrylamide or agarose gel for a short period (about 1.5-2 hr for a 15- to 20-cm gel). [4] The speed at which different molecules (and combinations thereof) move through the gel is determined by their size and charge, and to a lesser extent ...
Gasoline, Bunsen burners, and crucibles may also be used to evaporate and isolate substances in their dry forms. [4] [5] Wet chemistry is not performed with any advanced instruments since most automatically scan substances. [6] Although, simple instruments such as scales are used to measure the weight of a substance before and after a change ...
A NASA illustration of a lateral flow assay. A lateral flow test (LFT), [1] is an assay also known as a lateral flow immunochromatographic test (ICT), or rapid test.It is a simple device intended to detect the presence of a target substance in a liquid sample without the need for specialized and costly equipment.
C 0 t analysis, a technique based on the principles of DNA reassociation kinetics, is a biochemical technique that measures how much repetitive DNA is in a DNA sample such as a genome. [1]
Coupled assay for hexokinase using glucose-6-phosphate dehydrogenase. Even when the enzyme reaction does not result in a change in the absorbance of light, it can still be possible to use a spectrophotometric assay for the enzyme by using a coupled assay. Here, the product of one reaction is used as the substrate of another, easily detectable ...