Competitive Enzyme-Linked ImmunoSorbent Assay (ELISA) for the quantification of Microcystin concentration in accordance with EnviroLogix kit (Catalog Number EP 022).
This method calculates B/B0% of each sample using the negative control.
The standard data points (concentration vs. B/B0%) are plotted on semi-log axes and linear regression is fitted through the points. The concentrations of the samples are determined from the fit with any specified dilution factors applied.
The %CV, Standard Deviation and Standard Error are calculated for each replicated sample.
If the entire plate was read then supply the measured value for each well. Alternatively, if only specific parts of the plate were read then list only those measured values. In this case an additional step is required: under the Microplate section below, select or create a layout which defines which wells were read and which were not. More...
A zero concentration value has been specified with a logarithmic x axis.
This is valid but means that you will not see the zero standard on the chart, also in certain cases it may result in a skewed fit. One alternative is to use a suitably low value, such as 0.01 instead of zero. More...
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