• 제목/요약/키워드: brightfield

검색결과 2건 처리시간 0.013초

Utilization of Light Microscopy and FFT for MFA Measurement from Unstained Sections of Red Pine (Pinus Densiflora)

  • Kwon, Ohkyung;Lee, Mi-Rim;Eom, Chang-Deuk
    • Journal of the Korean Wood Science and Technology
    • /
    • 제41권5호
    • /
    • pp.399-405
    • /
    • 2013
  • This study demonstrates the utilization of light microscopy and Fast Fourier Transform-Peak Finding (FPF) method for microfibril angle (MFA) measurement from unstained sections of red pine (Pinus densiflora). To obtain an image with optimal contrast and resolution for MFA measurement, effects of numerical aperture (NA) of condenser lens and color filters were investigated. About 60% of NA of the maximum condenser NA produced an image with optimal contrast, but a color filter with short wavelength range (DAPI) created images with improved resolution. Manual angle measurement and the FPF method were applied to the image with optimal contrast for MFA measurement. The experimental results from the FPF method were considered to be more repeatable and less subjective than those from the manual angle measurement.

Multispectral intravital microscopy for simultaneous bright-field and fluorescence imaging of the microvasculature

  • Barry G. H. Janssen;Mohamadreza Najiminaini;Yan Min Zhang;Parsa Omidi;Jeffrey J. L. Carson
    • Applied Microscopy
    • /
    • 제51권
    • /
    • pp.12.1-12.12
    • /
    • 2021
  • Intravital video microscopy permits the observation of microcirculatory blood flow. This often requires fluorescent probes to visualize structures and dynamic processes that cannot be observed with conventional bright-field microscopy. Conventional light microscopes do not allow for simultaneous bright-field and fluorescent imaging. Moreover, in conventional microscopes, only one type of fluorescent label can be observed. This study introduces multispectral intravital video microscopy, which combines bright-field and fluorescence microscopy in a standard light microscope. The technique enables simultaneous real-time observation of fluorescently-labeled structures in relation to their direct physical surroundings. The advancement provides context for the orientation, movement, and function of labeled structures in the microcirculation.