However, there are several complexities built into the assay that can affect data interpretation.
Here we present a green fluorescent protein (GFP -based chromosomal reporter assay that can monitor both CAGFP -basedxpansions and chromosomals in the same human cell population.
However, accessing CSF is not a trivial task in a regular clinical setting, let alone in a screening assay that can be used for early-stage diagnosis.
Aiming to alleviate this problem, we developed a simple assay that can measure sialylation of transferrin directly from serum.
Successful control and eradication measures need a diagnostic assay that can distinguish between immune responses to infection and vaccination.
An assay that can identify multiple potyviruses simultaneously, with good specificity and sensitivity, is therefore highly desirable.
In an attempt to address the latter, we designed a novel assay that can identify de novo insulin synthesis.
Here we report the development of a single-molecule assay that can directly report head binding in a walking kinesin molecule, and show that only a single head is bound to the microtubule between steps at low ATP concentrations.
The nanoLAB addresses these needs and pushes the state of the art with sensitive 8-plex detection using a wash-free assay that can be run by anyone, anywhere.
In the new papers3,4 they go further, providing not only a link between the DNA and the protein it encodes, but also a functional assay that can handle large numbers of variants.
The Au NP films were further applied to the development of a sensitive assay that can detect influenza virus A (H1N1) and A (H3N2) at concentrations of 10 pg/ml and 10 PFU/ml respectively.
