Michael A Model

Summary

Affiliation: Kent State University
Country: USA

Publications

  1. ncbi Intensity calibration of a laser scanning confocal microscope based on concentrated dyes
    Michael A Model
    Department of Biological Sciences, Kent State University, Kent, Ohio, USA
    Anal Quant Cytol Histol 28:253-61. 2006
  2. ncbi Measurement of the absorption of concentrated dyes and their use for quantitative imaging of surface topography
    M A Model
    Department of Biological Sciences, Cunningham Hall, Kent State University, Kent, OH 44242, USA
    J Microsc 231:156-67. 2008
  3. ncbi 3D deconvolution of spherically aberrated images using commercial software
    M A Model
    Department of Biological Sciences, Kent State University, Kent, OH 44242, U S A
    J Microsc 241:94-100. 2011
  4. ncbi Measurement of wheat germ agglutinin binding with a fluorescence microscope
    Michael A Model
    Department of Biological Sciences, Kent State University, Kent, Ohio 44242, USA
    Cytometry A 75:874-81. 2009
  5. ncbi Thickness profiling of formaldehyde-fixed cells by transmission-through-dye microscopy
    Mariana Pelts
    Department of Biological Sciences, Kent State University, Kent, OH, USA
    Biotechniques 50:389-96. 2011
  6. ncbi Effect of modeled reduced gravity conditions on bacterial morphology and physiology
    Raja Vukanti
    Department of Biological Sciences, Kent State University, PO Box 5190, Kent, OH 44242, USA
    BMC Microbiol 12:4. 2012
  7. ncbi Measurement of bacterial volume by transmission-through-dye imaging
    Suzanne L Lababidi
    Department of Biological Sciences, Kent State University, Kent, OH 44242, USA
    J Microbiol Methods 87:375-7. 2011
  8. ncbi Intensity calibration and shading correction for fluorescence microscopes
    Michael A Model
    Kent State University, Kent, Ohio, USA
    Curr Protoc Cytom . 2006
  9. ncbi Measurement of the thickness and volume of adherent cells using transmission-through-dye microscopy
    Jennifer L Gregg
    School of Biomedical Sciences, Kent State University, Kent, OH 44242, USA
    Pflugers Arch 460:1097-104. 2010
  10. ncbi Difference between mean and threshold as a measure of intensity in confocal microscopy images
    Michael A Model
    Anal Quant Cytol Histol 28:341-3. 2006

Collaborators

  • Laura G Leff
  • J Fang
  • Y Chen
  • Mariana Pelts
  • Raja Vukanti
  • Suzanne L Lababidi
  • Jennifer L Gregg
  • Sahil M Pandya
  • Christine J Oh
  • Moumita Moitra
  • Karen M McGuire
  • Daniel C Focht

Detail Information

Publications10

  1. ncbi Intensity calibration of a laser scanning confocal microscope based on concentrated dyes
    Michael A Model
    Department of Biological Sciences, Kent State University, Kent, Ohio, USA
    Anal Quant Cytol Histol 28:253-61. 2006
    ..To find water-soluble fluorescent dyes with absorption in various regions of the spectrum and investigate their utility as standards for laser scanning confocal microscopy...
  2. ncbi Measurement of the absorption of concentrated dyes and their use for quantitative imaging of surface topography
    M A Model
    Department of Biological Sciences, Cunningham Hall, Kent State University, Kent, OH 44242, USA
    J Microsc 231:156-67. 2008
    ..At the same time, the interference pattern in the reflected image allows measurement of the refractive index of the dye...
  3. ncbi 3D deconvolution of spherically aberrated images using commercial software
    M A Model
    Department of Biological Sciences, Kent State University, Kent, OH 44242, U S A
    J Microsc 241:94-100. 2011
    ....
  4. ncbi Measurement of wheat germ agglutinin binding with a fluorescence microscope
    Michael A Model
    Department of Biological Sciences, Kent State University, Kent, Ohio 44242, USA
    Cytometry A 75:874-81. 2009
    ..For probes whose fluorescent properties are unaffected by binding, quantification of staining in true molecular units should be possible...
  5. ncbi Thickness profiling of formaldehyde-fixed cells by transmission-through-dye microscopy
    Mariana Pelts
    Department of Biological Sciences, Kent State University, Kent, OH, USA
    Biotechniques 50:389-96. 2011
    ..Quantification of cell thickness and volume on fixed cells is also possible during the early stages of fixation; this can be useful, for example, for measuring volume kinetics following rapid introduction of a stimulus...
  6. ncbi Effect of modeled reduced gravity conditions on bacterial morphology and physiology
    Raja Vukanti
    Department of Biological Sciences, Kent State University, PO Box 5190, Kent, OH 44242, USA
    BMC Microbiol 12:4. 2012
    ..The parameters selected have not been studied in E. coli and S. aureus under MRG conditions and provide critical information about bacterial viability and potential for population growth...
  7. ncbi Measurement of bacterial volume by transmission-through-dye imaging
    Suzanne L Lababidi
    Department of Biological Sciences, Kent State University, Kent, OH 44242, USA
    J Microbiol Methods 87:375-7. 2011
    ..The technique can be realized on any brightfield microscope and is applicable to bacteria of all shapes. TTD imaging requires that intact bacteria be immobilized on a flat transparent surface, such as a glass coverslip...
  8. ncbi Intensity calibration and shading correction for fluorescence microscopes
    Michael A Model
    Kent State University, Kent, Ohio, USA
    Curr Protoc Cytom . 2006
    ..The technique has a number of practical features that make it inexpensive, reproducible, and straightforward. Descriptions are given for both wide-field and confocal scanning fluorescence microscopy...
  9. ncbi Measurement of the thickness and volume of adherent cells using transmission-through-dye microscopy
    Jennifer L Gregg
    School of Biomedical Sciences, Kent State University, Kent, OH 44242, USA
    Pflugers Arch 460:1097-104. 2010
    ..To show possible applications of this method, we investigated the kinetics of the cell volume response to a hypotonic buffer and to the apoptotic agents staurosporine and ionomycin...
  10. ncbi Difference between mean and threshold as a measure of intensity in confocal microscopy images
    Michael A Model
    Anal Quant Cytol Histol 28:341-3. 2006