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For an applicable pH sensing the generated hybrid material is integrated in a microfluidic sensor chip setup.
Validation was performed by either ID-tag based multiple-primer DNA sequencing [5] or barcode hybridization, using our in-house microarray chip setup, the in-house barcode-chip.
The chip setup was randomized.
To further investigate the biocompatibility of PFPE Tris, we conducted an enzymatic activity assay in the droplets based on the previously developed REEAD (rolling-circle enhanced enzyme activity detection) on a chip setup.
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This is versus the current 3-chip setup consisting of the CPU, chipset (graphics, RAM, etc)., and the I/O.
This group later used carbon nanostrings to isotype transferrin isotypes in a lab-on-a-chip setup with a lateral flow strip (pI differences of 0.1 pH units could be successfully discriminated) [ 39].
Double emulsion droplets were generated using a two-microfluidic-chip setup where the w/o emulsions were first formed in an untreated PDMS chip and then fed to a hydrophilic (poly acrylic acid -coated) chip to generacid -coateduble emulsions.
Blank panels were used in order to accommodate the chip-setup.
This chip-type setup was characterized based on an electrophoresis expression of Nernst equation that was applied to the redox equilibrium of o-tolidine at different potentials.
As expected, beads this small are undetectable in this lens-free on-chip imaging setup.
Furthermore, the chip-based setup can be integrated with modules for DNA isolation in later versions.
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