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There, proper homodyne detection was achieved (mode matching of 90%).
In addition, a good selectivity for fructose detection was achieved.
Mass spectrometry detection was achieved by using electrospray ionization.
Detection was achieved with 3, 3'-diaminobenzidine (DAB, Zhongshan Golden Bridge Biotechnology Co., Ltd, Beijing, China) and counterstained with hematoxylin, dehydrated, cleared and mounted as in routine processing.
The electrochemical detection was achieved in both cases by the enzyme marker HRP.
Semi-quantitative detection was achieved through combining HCA and corresponding fitting curves.
The distribution of counts and the autocorrelation function for 200 fM monomer and 100 fM dimer demonstrate that single-molecule detection was achieved.
Therefore, a sensitive ratiometry for PSA detection was achieved with a linear range from 0.10 to 200 ng/mL.
As detection was achieved in the absence of added supporting electrolyte, the amperometric signal contains both faradic and capacitive components.
HGV RNA detection was achieved using primers specific for the 5′NCR and NS5a regions of the genome.
The sensitive detection was achieved by using the system consisted of G-riched DNA, blocker DNA, and the Nb.BbvCI biocatalyst.
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