### 10 assays found tagged with PerkinElmer

Time-resolved fluoroimmunoassay for the quantitative determination of total human thyroxine (T_{4}) in serum.

Time-resolved fluoroimmunoassay for the quantitative determination of human alpha-fetoprotein (hAFP) in serum.

Generic quantitative RIA for WIZARD2 CSV files.

Calculates IC50 values of samples measured at serial dilutions using the Four Parameter Fit method. Fits are overlaid for comparison.

Time-resolved fluoroimmunoassay for the quantitative determination of human free thyroxine (FT_{4}) in serum.

Quantitative analysis of samples using a Four Parameter Logistic (4PL) curve fit with 1/Y² data weighting in accordance with kit instructions. The standard data points (concentration vs. measurement) are plotted on log axes and a 4PL is fit through the points. The concentrations of the samples are determined from the fit with any specified dilution factors applied. The LDL is calculated by interpolating the average background counts (12 wells without analyte) + 3 x standard deviation value (average background counts + (3xSD)) on the standard curve. The %CV, Standard Deviation and Standard Error are calculated for each replicated sample. Samples outside the range of the standards or the fit (greater than the upper asymptote or below than the lower asymptote) are highlighted in yellow.

Quantitative analysis of samples using a Four Parameter Logistic (4PL) curve fit with 1/Y² data weighting in accordance with kit instructions. The standard data points (concentration vs. measurement) are plotted on log axes and a 4PL is fit through the points. The concentrations of the samples are determined from the fit with any specified dilution factors applied. The LDL is calculated by interpolating the average background counts (12 wells without analyte) + 3 x standard deviation value (average background counts + (3xSD)) on the standard curve. The %CV, Standard Deviation and Standard Error are calculated for each replicated sample. Samples outside the range of the standards or the fit (greater than the upper asymptote or below than the lower asymptote) are highlighted in yellow.

Time-resolved fluoroimmunoassay for the quantitative determination of human sex hormone-binding globulin (SHBG) in serum. The standard data points (concentration vs. measurement) are plotted on log-log axes and a cubic spline is fitted through the points. The concentrations of the samples are determined from the spline 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 (greater than the upper asymptote or below the lower asymptote) are highlighted in yellow.

Quantitative analysis of samples using a Four Parameter Logistic (4PL) curve fit with 1/Y² data suitable for AlphaLISA kits. The standard data points (concentration vs. measurement) are plotted on log axes and a 4PL is fit through the points. The concentrations of the samples are determined from the fit with any specified dilution factors applied. The LDL is calculated by interpolating the average background counts (12 wells without analyte) + 3 x standard deviation value (average background counts + (3xSD)) on the standard curve. The %CV, Standard Deviation and Standard Error are calculated for each replicated sample. Samples outside the range of the standards or the fit (greater than the upper asymptote or below than the lower asymptote) are highlighted in yellow.

Quantitative analysis of samples using a Four Parameter Logistic (4PL) curve fit with 1/Y² data suitable for AlphaLISA kits. The standard data points (concentration vs. measurement) are plotted on log axes and a 4PL is fit through the points. The concentrations of the samples are determined from the fit with any specified dilution factors applied. The LDL is calculated by interpolating the average background counts (12 wells without analyte) + 3 x standard deviation value (average background counts + (3xSD)) on the standard curve. The %CV, Standard Deviation and Standard Error are calculated for each replicated sample. Samples outside the range of the standards or the fit (greater than the upper asymptote or below than the lower asymptote) are highlighted in yellow.