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Dave Siak-Wei Ow

Researcher at Agency for Science, Technology and Research

Publications -  35
Citations -  792

Dave Siak-Wei Ow is an academic researcher from Agency for Science, Technology and Research. The author has contributed to research in topics: Gene & Gene expression. The author has an hindex of 13, co-authored 33 publications receiving 700 citations. Previous affiliations of Dave Siak-Wei Ow include National University of Singapore.

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Quantitative real-time polymerase chain reaction for determination of plasmid copy number in bacteria.

TL;DR: QPCR was found to show good reproducibility and high sensitivity in detecting a two fold difference in template concentration, and a wide linear dynamic range covering 0.5 pg to 50 ng of DNA.
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Global transcriptional analysis of metabolic burden due to plasmid maintenance in Escherichia coli DH5α during batch fermentation

TL;DR: It is suggested that plasmid maintenance alone perturbs global gene regulation, and leads to significant changes in central metabolic pathways in the host.
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Sonochemistry and sonoluminescence in microfluidics

TL;DR: This work presents a realization of sonoluminescence and sonochemistry created from bubbles confined within a narrow channel of polydimethylsiloxane-based microfluidic devices and finds the formation of OH radicals and the emission of light during bubble collapse.
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Creation of cavitation activity in a microfluidic device through acoustically driven capillary waves.

TL;DR: It is found that strong forcing leads to the excitation of nonlinear surface waves when gas-liquid interfaces are present in the microfluidic channels and nuclei leading to intense inertial cavitation are generated by the entrapment of gas pockets at those interfaces.
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Sonolysis of Escherichia coli and Pichia pastoris in microfluidics

TL;DR: An efficient ultrasound based technique for lysing Escherichia coli and Pichia pastoris with oscillating cavitation bubbles in an integrated microfluidic system and qRT-PCR analysis show that functionality of GFP and genomic DNA for downstream analytical assays is maintained.