What is the maximum sample throughput?

Where can I find a standard curve for the proteins I have run?

Why do some of your biomarkers have several Uniprot numbers?

Why do the negative control and interplate control samples flag/not pass the quality control (QC)?

Why is the limit for a sample passing or failing the quality control set to +/- 0.3NPX of the plate median for Incubation control 2 and the detection control?

Why would a sample not pass quality control in only one out of several panels run?

What do LLOQ and ULOQ mean?

How should total protein concentration in cell and tissue lysates be determined?

Are internal controls included in the assay, and if so what are they?

How is the data pre-processed?