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The assay was designed to cover the concentration range 0.5 to 50 ng/ml.
The assay was designed to the Internal Transcribed Spacer 2 region of the Trichinella genome.
The assay was designed to amplify the VP72 gene of ASFV genome.
The assay was designed to allow for simultaneous comparison of CYP1A expression among each experimental group.
The assay was designed by integrating the Au nanoparticles (NPs) labeled probe DNA (pDNA-Au) with CdSe quantum dots (QDs).
The assay was designed to detect S-adenosylhomocysteine (AdoHcy), a product of all S-adenosylmethionine (AdoMet -utilizing methyltrAdoMet -utilizingns.
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The assay is designed against the 9GL region and is capable of detecting 20 copies of a DNA standard.
The assay is designed to be both simple and economical to enable its use in the field.
Based on this general principle, the assay is designed to detect and identify protein binding partners of a protein complex.
The assay is designed to facilitate the efficient screening for novel inhibitory chemical compounds or peptides in a simple flow cytometry-based platform.
The assay is designed to produce a linear analytical response from at least 100 20,000 cells per well in most cell lines.
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CEO of Professional Science Editing for Scientists @ prosciediting.com