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A Novel Utility to Correct for Plate/Batch/Lot and Nonspecific Binding Artifacts in Luminex Data

Cytokines and other secreted soluble proteins are routinely assayed as fluorescence intensities on the Luminex (Luminex, Austin, TX) platform. As with any immunoassay, a portion of the measured Ab binding can be nonspecific. Use of spiked-in microbead controls (e.g., AssayChex Process, Control Panel...

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Podrobná bibliografie
Vydáno v:J Immunol
Hlavní autoři: Maecker, Holden T., Rosenberg-Hasson, Yael, Kolstad, Kathleen Durgin, Steen, Virginia D., Chung, Lorinda S.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2020
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7891557/
https://ncbi.nlm.nih.gov/pubmed/32376648
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4049/jimmunol.2000017
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