Assay Setup
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Why do the negative control and interplate control samples flag/not pass the quality control (QC)?
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How many replicates of each sample are analyzed?
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Should I dilute my samples before shipping them to Olink?
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Why would a sample not pass quality control in only one out of several panels run?
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I see that the same protein can be measured by more than one panel, are these the same assay?
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How is it determined whether a sample has failed quality control because of operator error or due to some property of the sample?
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Why do some of your biomarkers have several Uniprot numbers?
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Is it possible to run formalin fixed samples with Olink?
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What is the maximum sample throughput?
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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?