1
Main outcome measures: Results of a polymerase chain reaction- based assay for genotyping.
2
In this paper, the issue was approached by using a reporter- based assay.
3
We present general means to greatly increase the sensitivity of antibody- based assays.
4
The coagulation- based assays gave the best correlation to in vivo antithrombotic activity.
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Plasma markers of innate immune activation were measured using standard ELISA- based assays.
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Several of these analogs were potent VEGF inducers in a cell- based assay.
7
Classically, the study of histone variants has largely relied on antibody- based assays.
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Protein synthesis and fatty acid oxidation were measured by radioactive tracer- based assays.
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The epitope off-rate was evaluated by gel filtration and T cell- based assays.
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Subvariant type was assigned by a combination of PCR-restriction fragment length polymorphism- based assays.
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The addition of KCTD16 improves the sensitivity of the cell- based assay.
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Third, a methylation-sensitive quantitative PCR- based assay was performed on a subset of samples.
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Background: PCR- based assays can improve clinical care, but they remain technically demanding and labor-intensive.
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Here we describe a sensitive and specific radioactivity- based assay to measure PI kinase activity.
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Phenotypic and functional studies of Blimp-1-expressing T cells were performed using flow cytometry- based assays.
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In addition, we utilized a fast NMR- based assay for the generation of I-domain-inhibitor models.