Quantitative determination of Anti-Mullerian Hormone (AMH) levels in serum and lithium heparin plasma for Gen II ELISA kit. The standard data points are plotted (concentration vs. absorbance measurement) and a cubic regression curve is fitted through these 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. Samples outside the range of the standards or the fit are highlighted in yellow.

Quantitative determination of Anti-Mullerian Hormone (AMH) levels in serum and lithium heparin plasma for Gen II ELISA kit. The standard data points are plotted (concentration vs. absorbance measurement) and a Four Parameter Logistic Fit (4PL) is made through these points. The concentrations of the samples are determined from the fit. It is important to note that concentrations can only be determined for samples which fall within the range of the determined upper and lower asymptotes of the fit (the a and d parameters).

Enzyme linked immunosorbent assay (ELISA) for the quantitative measurement of Inhibin B in serum and lithium heparin plasma. This method calculates the mean absorbance for each standard (calibrator), control and sample. The blank corrected mean absorbances are plotted against the concentration values on log axes. Linear regression is used to determine the concentration of the samples. Any specified dilution factors are applied. Samples are outside the range of the standards are highlighted in yellow and should be reassayed in accordance with the kit instructions.

Enzyme linked immunosorbent assay (ELISA) for the quantitative measurement of Inhibin B in serum and lithium heparin plasma. This method calculates the mean absorbance for each standard (calibrator), control and sample. The blank corrected mean absorbances are plotted against the concentration values on log axes. Cubic regression is used to determine the concentration of the samples. Any specified dilution factors are applied. Samples are outside the range of the standards are highlighted in yellow and should be reassayed in accordance with the kit instructions.

Enzyme linked immunosorbent assay (ELISA) for the quantitative measurement of Inhibin B in serum and lithium heparin plasma. This method calculates the mean absorbance for each standard (calibrator), control and sample. The blank corrected mean absorbances are plotted against the concentration values on log axes. The Four Parameter Logistic Fit is used to determine the concentration of the samples. Any specified dilution factors are applied. Samples are outside the range of the standards are highlighted in yellow and should be reassayed in accordance with the kit instructions.

Competition enzyme immunoassay of histamine. This method calculates the mean absorbance for each standard (calibrator), control and sample. If a blank group is defined on the layout the mean of the blank measurements is used to background correct the absorbance values. The mean absorbances are plotted against the concentration values on log axes. A Four Parameter Logistic Fit is used to determine the concentration of the samples. Any specified dilution factors are applied. Samples are outside the range of the standards are highlighted in yellow and should be reassayed in accordance with the kit instructions.