David Charlot, PhD, MSEng

David Charlot, PhD, MSEng

Newark, New Jersey, United States
11K followers 500+ connections

Experience

  • AuraSense™ Graphic

    AuraSense™

    Newark, New Jersey, United States

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    Irvine, California, United States

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    Washington, District of Columbia, United States

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    Tempe, Arizona, United States

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    Boston, Massachusetts, United States

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    Washington, District of Columbia, United States

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    Garden Grove, California

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    San Diego, California

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    San Diego, California

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    La Jolla, California

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    La Jolla, California

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    La Jolla, California

Education

  • UC San Diego Graphic

    UC San Diego

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    Graduate Research Associate, Jeff Price Quantitative Microscopy Lab, 2006-2010
    Developed high content screening instrumentation for drug discovery related to oncology, heart disease and stem cell differentiation.

    Key Contributions:
    * Built continuous scanning fluorescence microscope instrument using laser autofocus, time delay and integrate ccd technology, and multi-spectral LED illumination to increase chemical compound high content screening throughput for drug discovery by…

    Graduate Research Associate, Jeff Price Quantitative Microscopy Lab, 2006-2010
    Developed high content screening instrumentation for drug discovery related to oncology, heart disease and stem cell differentiation.

    Key Contributions:
    * Built continuous scanning fluorescence microscope instrument using laser autofocus, time delay and integrate ccd technology, and multi-spectral LED illumination to increase chemical compound high content screening throughput for drug discovery by 8-fold.
    * Created inaugural Kinetic Image Cytometer for automated capture and analysis of calcium transients in cell cultures for stem cell research, drug discovery and toxicity studies and installed in stem cell core facility at Sanford Burnham Prebys Institute.
    * Presented scientific findings at conferences and generated unique IP for calcium transient image cytometry.
    * Supervised 2 graduate students.

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    Grader and Teaching Assistant, 2005-2007
    Assisted professors in Introduction to Bioengineering Design, Bioengineering Mass Transfer, Continuum Mechanics, and Biomechanics classes.

    Graduate Research Associate, Michael Berns Robolase Lab, 2006
    Built optical laser tweezer fluorescence microscope system to chart effects of shear stress on epithelial cell membrane and cytoplasm. Correlated change in optical power density of laser tweezers with viscosity and deformation of the cells’…

    Grader and Teaching Assistant, 2005-2007
    Assisted professors in Introduction to Bioengineering Design, Bioengineering Mass Transfer, Continuum Mechanics, and Biomechanics classes.

    Graduate Research Associate, Michael Berns Robolase Lab, 2006
    Built optical laser tweezer fluorescence microscope system to chart effects of shear stress on epithelial cell membrane and cytoplasm. Correlated change in optical power density of laser tweezers with viscosity and deformation of the cells’ membrane through real-time live cell imaging.

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    Activities and Societies: Minority Access to Research Careers (MARC) Scholar, 2002-2004 Leadership Summer Research - Early Identification Program, 2003 (University of Colorado Boulder) Summer Research Experience for Undergraduates, 2002 (The College of William and Mary)

    I studied General Physics with Medical Emphasis

Volunteer Experience

  • AES Electrophoresis Society Graphic

    President Elect

    AES Electrophoresis Society

    - 2 years 10 months

    Science and Technology

    AES Electrophoresis Society is a unique, non-profit, international organization founded to advance and promote electric field-mediated separations, manipulations, and related phenomena. The field of electrokinetics intersects microfluidics and microdevices, biotechnology, theoretical modeling, material synthesis, nanotechnology and many others. Electrophoretic technologies play a central role in scientific investigations in clinical, basic, and applied disciplines from life sciences through…

    AES Electrophoresis Society is a unique, non-profit, international organization founded to advance and promote electric field-mediated separations, manipulations, and related phenomena. The field of electrokinetics intersects microfluidics and microdevices, biotechnology, theoretical modeling, material synthesis, nanotechnology and many others. Electrophoretic technologies play a central role in scientific investigations in clinical, basic, and applied disciplines from life sciences through chemistry and physics, to engineering. Our goal is to promote excellence in electrokinetic technologies, thus improving the overall quality and sophistication of scientific research.

    The AES Electrophoresis Society:

    Is dedicated to the development and refinement of electrokinetic and related technologies;
    Was formed to promote excellence, generate scientific knowledge, and engineer techniques;
    Facilitates collaboration and communication among members worldwide; and
    Enhances development of students and professionals

    Key Contributions:
    Creation / development of workshops teaching organization members process development strategy applied to research and technical communication
    Expanding collaboration with other STEM based non-profit organizations to increase member awareness
    Development of presentation tracks that show STEM opportunities beyond academic career track

  • AES Electrophoresis Society Graphic

    Councilor

    AES Electrophoresis Society

    - 2 years 1 month

    Science and Technology

Publications

  • Automated calcium measurements in live cardiomyocytes

    IEEE

    Heart failure due to hypertension, infarction, or other factors, is a leading killer of men and women in modern society and involves, at its base, a debilitating loss of cardiomyocytes. Recent studies indicate the feasibility of regenerating lost cardiomyocytes by transplanting embryonic stem cell-derived cardiomyocytes (ESCMs) or mobilizing resident stem cells. To realize the potential of stem-cell based therapies, we hypothesize that it will be extremely beneficial to develop technology and…

    Heart failure due to hypertension, infarction, or other factors, is a leading killer of men and women in modern society and involves, at its base, a debilitating loss of cardiomyocytes. Recent studies indicate the feasibility of regenerating lost cardiomyocytes by transplanting embryonic stem cell-derived cardiomyocytes (ESCMs) or mobilizing resident stem cells. To realize the potential of stem-cell based therapies, we hypothesize that it will be extremely beneficial to develop technology and instruments for high throughput, high content screening (HCS) of drugs and genes for their ability to stimulate the formation of functional, contractile cardiomyocytes. Contractile activity is the primary physiological function of cardiomyocytes and abnormal contractility is potentially lethal. We discuss the first phase of the development of an instrument dedicated to distinguishing differentiated ESCMs from undifferentiated non-cardiac background cells using automated cell-by-cell quantification of contractile-calcium transients as the primary assay.

    Other authors
    See publication
  • Exact Analytical and Numerical Calculation of the Radiative Recombination Cross Sections of Fully Stripped Ions

    Journal of Electromagnetic Waves and Applications

    Analytical expressions for the direct radiative recombination (RR) cross section are derived within a non-relativistic treatment in the dipole approximation for hydrogenic systems with one electron at any given incident energy.

    Other authors

Patents

  • Devices for Separation of Biological Materials

    Issued US 9,387,486

    The present invention includes methods, devices and systems for isolating nanoparticulates, including nucleic acids, from biological samples. In various aspects, the methods, devices and systems may allow for a rapid procedure that requires a minimal amount of material and/or results in high purity isolation of biological components from complex fluids such as blood or environmental samples.

    Other inventors
    See patent
  • Nucleic acid sample preparation

    Issued US 9,206,416

    The present invention includes methods, devices and systems for isolating a nucleic acid from a fluid comprising cells. In various aspects, the methods, devices and systems may allow for a rapid procedure that requires a minimal amount of material and/or results in high purity nucleic acid isolated from complex fluids such as blood or environmental samples.

    Other inventors
    See patent
  • Nucleic acid sample preparation

    Issued US 9,034,579

    The present invention includes methods, devices and systems for isolating a nucleic acid from a fluid comprising cells. In various aspects, the methods, devices and systems may allow for a rapid procedure that requires a minimal amount of material and/or results in high purity nucleic acid isolated from complex fluids such as blood or environmental samples.

    Other inventors
    See patent
  • Automated transient image cytometry

    Issued US 8,385,624

    A method, system, and instrument for automatically measuring transient activity in cells uses image time sequences to identify transients in cells. Preferably, the transient activity is stimulated or provoked in synchronism with acquisition of the image time sequences. A cell mask is applied to each image of an image time sequence in order to localize the transient activity with respect to each cell. Localization enables cell-by-cell analysis of properties of the transient activity.

    Other inventors
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  • MANIPULATION OF MICROPARTICLES IN LOW FIELD DIELECTROPHORETIC REGIONS

    Filed US 20150219618 A1

    The present invention includes methods, devices and systems for isolating a target biological material from a biological sample. In various aspects, the methods, devices and systems may allow for a rapid procedure that requires a minimal amount of material and/or results in isolated target biological material from complex fluids such as blood or environmental samples.

    See patent

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