Standing wave microscopy of red blood cell membrane morphology with high temporal resolution

Tinning, Peter W. and Scrimgeour, Ross and McConnell, Gail (2018) Standing wave microscopy of red blood cell membrane morphology with high temporal resolution. In: 18th European Light Microscopy Initiative Meeting 2018, 2018-06-05 - 2018-06-08.

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Abstract

Widefield fluorescence microscopy is an integral tool for life science imaging though the achievable resolutions are limited by the diffraction nature of light. One technique to increase the axial resolution is known as standing wave microscopy [1]. The standing wave can be generated by placing a mirror at the specimen plane which causes interference between the incoming and reflected excitation illumination. The axial resolution is reduced to λ/4n as only fluorophores which are in the location of the full width at the half maximum of the antinodes are excited [2] resulting in periodic bands of fluorescence.

ORCID iDs

Tinning, Peter W. ORCID logoORCID: https://orcid.org/0000-0002-3270-4120, Scrimgeour, Ross ORCID logoORCID: https://orcid.org/0000-0003-1412-9748 and McConnell, Gail ORCID logoORCID: https://orcid.org/0000-0002-7213-0686;
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