Locking in on large volume light-sheet microscopy

TY - CONF

T1 - Locking in on large volume light-sheet microscopy

AU - Vettenburg, T.

AU - Dalgarno, H. I. C.

AU - Nylk, J.

AU - Coll-Llado, C.

AU - Ferrier, D. E. K.

AU - Cizmar, T.

AU - Gunn-Moore, F. J.

AU - Dholakia, K.

AU - Corral, A.

AU - Rodriguez-Pulido, A.

AU - Flors, C.

AU - Ripoll, J.

N1 - Conference code: 16

PY - 2018/6/4

Y1 - 2018/6/4

N2 - Fluorescence light-sheet microscopy is increasingly adopted by developmental biologists to study how cells divide and differentiate to form organs and even entire organisms. The light-sheet microscope differs from a conventional microscope in that the specimen is illuminated by a plane of light orthogonal to the detection axis, thus keeping the out-of-focus areas dark while minimizing any potentially detrimental exposure of the sample. The light-sheet microscope has been found to be the ideal instrument for long-term and non-invasive studies of intact, and therefore three-dimensional, fluorescent samples.

AB - Fluorescence light-sheet microscopy is increasingly adopted by developmental biologists to study how cells divide and differentiate to form organs and even entire organisms. The light-sheet microscope differs from a conventional microscope in that the specimen is illuminated by a plane of light orthogonal to the detection axis, thus keeping the out-of-focus areas dark while minimizing any potentially detrimental exposure of the sample. The light-sheet microscope has been found to be the ideal instrument for long-term and non-invasive studies of intact, and therefore three-dimensional, fluorescent samples.

UR - http://hdl.handle.net/11104/0287640

M3 - Abstract

SP - 84

EP - 85

T2 - Recent Trends in Charged Particle Optics and Surface Physics Instrumentation

Y2 - 4 June 2018 through 6 June 2018

ER -