2026-09-19T00:26:26Zhttps://dspace.mit.edu/server/oai/requestoai:dspace.mit.edu:1721.1/611482022-01-13T07:54:29Zcom_1721.1_7582com_1721.1_7581col_1721.1_131023
Edward S. Boyden.
Chang, Jeremy T
Massachusetts Institute of Technology. Dept. of Electrical Engineering and Computer Science.
Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
2011-02-23T14:20:31Z
2011-02-23T14:20:31Z
2010
2010
http://hdl.handle.net/1721.1/61148
698127201
Thesis (M. Eng.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2010.
Cataloged from PDF version of thesis.
Includes bibliographical references (p. 45-46).
Fast scanning two-photon microscopy coupled with the use light activated ion channels provides the basis for fast imaging and stimulation in the characterization of in vivo neural networks. A two-photon microscope capable of fast scanning using acousto-optic deflectors was designed and implemented. The software controller was expanded so that random access scan in three dimensions could be handled, so that algorithms that can identify neurons from images acquired using the two-photon microscope can be developed. Finally the localization of optogenetic Channelrhodopsin-2 channel to the neuron cell body was tested using a ChR2-MBD construct.
by Jeremy T Chang.
M.Eng.
46 p.
eng
Massachusetts Institute of Technology
M.I.T. theses are protected by
copyright. They may be viewed from this source for any purpose, but
reproduction or distribution in any format is prohibited without written
permission. See provided URL for inquiries about permission.
http://dspace.mit.edu/handle/1721.1/7582
Electrical Engineering and Computer Science.
Fast scanning two-photon microscopy
Fast scanning 2-photon microscopy
Fast scanning two-photon microscope
Thesis
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Publication
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