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Both assays are based on a magnetically induced direct electrochemical detection of gold tags on magnetic graphite-epoxy composite electrodes.
These assays are based on recognition of mycobacterial DNA sequences and the subsequent amplification of nucleic acid sequences to facilitate detection.
These assays are based on the observation that a given protein can be split into two inactive fragments and these fragments can reassemble into the original properly folded and functional structure.
Unless otherwise mentioned, the molar concentrations of ClpX in the various assays are based on monomer molecular weight.
These assays are based on the principle that antibody response to HIV infection matures over time and that immunological biomarkers of HIV disease progression can be used to distinguish recent from non-recent HIV infection.
These assays are based on completely different principles.
These assays are based on the fluorescence of products generated from substrate hydrolysis by the enzyme.
These assays are based on those previously described by Farzan and co-workers.
These assays are based on a solid-phase sandwich ELISA using specific anti-BACE or anti-APP antibodies.
These assays are based on spectrophotometric quantification of a color compound that forms in response to oxidation.
These assays are based on the fluorescence of products generated from the hydrolysis of the substrate by the enzyme.
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