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The classical phenol chloroform extraction method allowed for the PCR with the lowest detection limit.
This method allowed for the determination of the active zones in the reactor.
A simple wrinkling method allowed for a spatial resolution <1.5 μm by converting the wrinkling frequency.
This method allowed for isolation of stage-specific embryonic antigen-3-positive (SSEA-3+) and SSEA-3 cells from hESC cultures.
This method allowed for the incorporation of the two antigens into a polymeric dendrimer in a strictly equimolar ratio.
Further, the iterative implementation of this method allowed for high quality reconstruction of susceptibility maps of human brain in vivo.
The developed method allowed for accurate assessment of prognosis in prostate cancer patients who underwent radical prostatectomy.
The spatial stability introduced by this method allowed for long term measurements of oxygen tension without interfering with the cell aggregation process.
Our method allowed for us (1) to get data through the conversion of optical luminance into numerical values and (2) to accurately measure image features through numerical analysis.
The automation of the method allowed for fast reduction and optimization of seven experimental data sets which were then validated by process simulation.
This method allowed for quantitative detection of GDH with a detection limit of 1 nM, providing great potential for its further application in CDI diagnosis.
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