Sentence examples for amplified sensitivity from inspiring English sources
Greatly amplified sensitivity was achieved by using GR-TH/HNP-PtCu composite owing to its large specific surface and good electron-transfer ability.
Results from piezoresistivity experiments confirm that the nanoreinforced mortars exhibit an increased change in resistivity under cyclic compressive loading, which is indicative of the amplified sensitivity of the material in strain sensing.
The reasons for such ultrahigh and amplified sensitivity can be attributed to the use of GO and streptavidin-modified Au NPs which not only improved the electron transfer rate, but also increased the amount of capture anti-p53.
A novel amperometric enzyme immunosensor with amplified sensitivity for the determination of alpha-fetoprotein (AFP) was constructed with layer-by-layer assembly of ZnSe quantum dots (ZnSe QDs)/Azure I/gold nanoparticles (nanoAu /poly (3,4-ethylenedioxythiophene) (PEDOT) on Pt electrode.
Using α-1-fetoprotein (AFP) as a model, this novel immunosensor presented amplified sensitivity, good stability, and a broader linear response in two ranges from 0.5 20 ng/mL and 20 200 ng/mL with a detection limit of 0.26 ng/mL, as well as good selectivity and storage stability.
Insulin was analysed by a solid phase enzyme amplified sensitivity immunoassay (Medgenix INS-ELISA, Biosource, Belgium).
Serum insulin levels were measured in duplicate by monoclonal immunoradiometric assay (or enzyme-amplified sensitivity immunoassay [EASIA], Medgenix Diagnostics, Fleunes, Belgium).
The induction of metalloproteinase-3 and proteoglycan synthesis was evaluated by a solid-phase enzyme-amplified sensitivity immunoassay, and nitric oxide production was evaluated with the Griess method.
STNFR-1 EASIA (normal range: 3.4 to 10.8 ng/mL; intra-assay variation: 1.7%) are solid phase enzyme-amplified sensitivity immunoassays performed on a microtiter plate (, Biosource Technologies, Inc., Fleunes, Belgium).
It is a solid-phase, enzyme-amplified sensitivity immunoassay performed on microtiter plates based on the oligoclonal system in which several monoclonal antibodies directed against distinct epitopes of cytokines are used, permitting a high sensitivity of the assay.
The quantity of PGs was measured in the culture medium by a solid-phase enzyme-amplified sensitivity immunoassay (EASIA DIAsource ImmunoAssay SASA, Nivelles, Belgium), performed on microtiter plates (Heinegard and Saxne 13).
