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Is it possible to run formalin fixed samples with Olink?
How will PEG (polyethylene glycol) in the samples affect the assays and the results?
How should total protein concentration in cell and tissue lysates be determined?
What throughput is offered by using the Olink panels?
How do you perform reverse pipetting?
What is reverse pipetting?
What is the optimal starting concentration for cell and tissue lysates?
Is sample dilution necessary before running the assay?
Protein data points generated
Publications listed on website
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