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Using this assay, we demonstrate that some apoptotic cells transform into necrotic phenotypes, with a delay of 30 min to 3 h.
Using this assay, we reproducibly detected as little as 5 nM guanine.
Using this assay, we then tested 44 human primary colorectal tumors.
Using this assay, we assessed 16 mutations reported in MEK1, a MAPK kinase, and provide a robust ranking of these mutations.
Using this assay, we identified ATP5B, a core subunit of the mitochondrial ATP synthase, as having high affinity to the RV 3'UTR consensus sequences.
Using this assay, we were able to identify gene amplifications and deletions genome-wide and with high resolution, and compare alterations in DNA copy number and gene expression.
Using this assay, we demonstrated that p97/Gab2 specifically interacts with the SH2 domains of PI3K, SHP-2 and CrkL.
Using this assay, we determined the Km of two acceptor substrates, N-acetyl-l-lysine methyl ester and aminoacetonitrile.
To determine whether we could monitor expansions using this assay, we sorted GFP− and GFP+ cells from a population of GFP CAG 101 cells using fluorescence-activated cell sorting (FACS).
Using this assay, we analyzed human blood samples from the Wosera (n = 703) and Mugil (n = 986) regions to evaluate the prevalence of these P. vivax strains.
Using this assay we found that the number of sjTRECs in peripheral blood mononuclear cells was less than 10% that of the thymus.
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using this methodology we
using this strategy we
using this remark we
using this dataset we
using this process we
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using this equation we
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using this logic we
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com