Cutaneous metastasis of gastric signet ring cell carcinoma masquerading as allergic contact dermatitis.
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Biomedical subjects
Publications and source records attributed to Sang-Hyun Oh.
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Protein microarray technology, in which a large number of capture ligands are spatially arrayed at a high density, presents an attractive method for high-throughput proteomic analysis. Toward this end, we demonstrate the first cell-based protein detection in a microsystem, wherein Escherichia coli cells are genetically engineered to express the desired capture proteins on the membrane surface and are spatially arrayed as sensing elements in a microfluidic device. An E. coli clone expressing peptide ligands with high affinity and high specificity for target molecules was isolated a priori. Then these cells were electrokinetically immobilized on gold electrodes using dielectrophoresis, thus allowing each sensor element to be electrically addressable. Flow cytometry and subsequent fluorescence analysis verified the highly specific capture and detection of target molecules by the bacteria. Finally, through the coexpression of peptide-based capture ligands on the cell surface and fluorescent protein in the cytoplasm, we demonstrate an effective means of directly linking the fluorescence intensity to the density of capture ligands.
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Free-space-based channelized dynamic spectral equalizers are theoretically investigated by solving the temporal-frequency-dependent power-coupling integral for commonly used active device technologies: liquid-crystal modulators, tilting micromirror arrays, and deformable gratings. Channel-filter characteristics, such as bandwidth and interchannel transition, are found to depend on the different attenuation mechanisms provided by the active devices. Such information is required for choosing the proper device parameters in designing channel equalizers and similar free-space spatially dispersed subsystems.