TY - JOUR
T1 - Optical clearing of fixed brain samples using SeeDB
AU - Ke, Meng Tsen
AU - Imai, Takeshi
N1 - Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2014
Y1 - 2014
N2 - Large-scale three-dimensional fluorescence imaging is essential for comprehensive and quantitative understanding of neuronal circuitry.We describe a water-based optical clearing agent, SeeDB, which clears fixed brain samples in a few days leaving many types of fluorescent dyes unquenched, including fluorescent proteins and lipophilic neuronal tracers. This method maintains a constant sample volume during the clearing procedure, an important factor to keep cellular morphology intact. After optical clearing with SeeDB, we can reach a depth of >1000 μm with confocal microscopy. When combined with two-photon microscopy, SeeDB allows us to image fixed mouse brains at millimeter-scale level.
AB - Large-scale three-dimensional fluorescence imaging is essential for comprehensive and quantitative understanding of neuronal circuitry.We describe a water-based optical clearing agent, SeeDB, which clears fixed brain samples in a few days leaving many types of fluorescent dyes unquenched, including fluorescent proteins and lipophilic neuronal tracers. This method maintains a constant sample volume during the clearing procedure, an important factor to keep cellular morphology intact. After optical clearing with SeeDB, we can reach a depth of >1000 μm with confocal microscopy. When combined with two-photon microscopy, SeeDB allows us to image fixed mouse brains at millimeter-scale level.
UR - http://www.scopus.com/inward/record.url?scp=84905694063&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84905694063&partnerID=8YFLogxK
U2 - 10.1002/0471142301.ns0222s66
DO - 10.1002/0471142301.ns0222s66
M3 - Article
C2 - 24510778
AN - SCOPUS:84905694063
SN - 1934-8584
JO - Current Protocols in Neuroscience
JF - Current Protocols in Neuroscience
IS - SUPPL.66
M1 - 2.22
ER -