Welcome to our library of frequently asked questions!
The FAQs are grouped into categories of related topics for your convenience:
– Click the category title to see the associated FAQs
– The number of questions in each category shown in the blue boxes
In case your question is not answered here, an enquiry form is available on each of the individual FAQs
Search all our FAQs
How is the Limit of Detection (LOD) estimated and how is this handled in the data analysis?
Why would a sample not pass quality control in only one out of several panels run?
Should I dilute my samples before shipping them to Olink?
How many replicates of each sample are analyzed?
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?
What is the maximum sample throughput for Olink Target?
Where can I find a standard curve for the proteins I have run?
How is it determined whether a sample has failed quality control because of operator error or due to some property of the sample?
I see that the same protein can be measured by more than one panel, are these the same assay?
Protein data points generated
Publications listed on website