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Séminaire de la FFJ à l'ISMO : Sarah Abrahamsson

2023-03-21 11:00 2023-03-21 12:00 Séminaire de la FFJ à l'ISMO : Sarah Abrahamsson

Deep volume 3D imaging with a 25-camera array multifocus microscope

par Sarah Abrahamsson

University of California Santa Cruz

The conflict between the three-dimensional nature of the world and the two-dimensionality of the microscope image is a classical problem in biological imaging and in the field of Optics. Aberration-corrected multifocus microscopy (MFM) uniquely addresses this problem by truly simultaneously acquiring data from multiple planes of an object at the full resolution that the optical microscope can attain. Using diffractive Fourier optics, the image beam from a wide-field microscope is multiplexed and refocused and the 3D focal stack is captured on one or multiple high-speed cameras. MFM is compatible with super-resolution and localization microscopy and provides high-speed 3D imaging of living specimens without the need for image reconstruction. Applications of MFM range from functional neuronal imaging in small model organisms to visualizing transcription inside the cell nucleus.
Contact pour demander le lien :
http://www.ismo.universite-paris-saclay.fr/spip.php?article2778

bât 520
Thematique : Recherche

Deep volume 3D imaging with a 25-camera array multifocus microscope

  • Public
    Réservé à certains publics
  • Type d'évènement
    Conférence / séminaire / webinaire
  • Dates
    Mardi 21 mars, 11h00
    11:00 am - 12:00 pm
  • Lieu
    bât 520

Deep volume 3D imaging with a 25-camera array multifocus microscope

par Sarah Abrahamsson

University of California Santa Cruz

The conflict between the three-dimensional nature of the world and the two-dimensionality of the microscope image is a classical problem in biological imaging and in the field of Optics. Aberration-corrected multifocus microscopy (MFM) uniquely addresses this problem by truly simultaneously acquiring data from multiple planes of an object at the full resolution that the optical microscope can attain. Using diffractive Fourier optics, the image beam from a wide-field microscope is multiplexed and refocused and the 3D focal stack is captured on one or multiple high-speed cameras. MFM is compatible with super-resolution and localization microscopy and provides high-speed 3D imaging of living specimens without the need for image reconstruction. Applications of MFM range from functional neuronal imaging in small model organisms to visualizing transcription inside the cell nucleus.
Contact pour demander le lien :
http://www.ismo.universite-paris-saclay.fr/spip.php?article2778