dc.contributor.author |
Soeller, Christian |
en |
dc.contributor.author |
Jacobs, MD |
en |
dc.contributor.author |
Donaldson, Paul |
en |
dc.contributor.author |
Cannell, Mark |
en |
dc.date.accessioned |
2011-09-04T23:49:59Z |
en |
dc.date.issued |
2003 |
en |
dc.identifier.citation |
J Biomed Opt 8(3):418-427 Jul 2003 |
en |
dc.identifier.issn |
1083-3668 |
en |
dc.identifier.uri |
http://hdl.handle.net/2292/7632 |
en |
dc.description |
One print or electronic copy may be made for personal use only. Systematic reproduction and distribution, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper are prohibited. |
en |
dc.description.abstract |
Two-photon excitation makes it possible to excite molecules in volumes of much less than 1 fl. In two-photon flash photolysis (TPFP) this property is used to release effector molecules from caged precursors with high three-dimensional resolution. We |
en |
dc.language |
EN |
en |
dc.relation.ispartofseries |
Journal of Biomedical Optics |
en |
dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.sherpa.ac.uk/romeo/issn/1083-3668/ |
en |
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
en |
dc.rights.uri |
http://spie.org/x85011.xml |
en |
dc.subject |
two-photon |
en |
dc.subject |
photolysis |
en |
dc.subject |
microscopy |
en |
dc.subject |
calcium |
en |
dc.subject |
diffusion |
en |
dc.subject |
caged compounds |
en |
dc.subject |
GAP JUNCTION CHANNELS |
en |
dc.subject |
FROG SKELETAL-MUSCLE |
en |
dc.subject |
CALCIUM-RELEASE |
en |
dc.subject |
CAGED COMPOUNDS |
en |
dc.subject |
LIVING CELLS |
en |
dc.subject |
QUANTITATIVE-DETERMINATION |
en |
dc.subject |
DYE TRANSFER |
en |
dc.subject |
DIFFUSION |
en |
dc.subject |
LENS |
en |
dc.subject |
FLUORESCENCE |
en |
dc.title |
Application of two-photon flash photolysis to reveal intercellular communication and intracellular Ca2+ movements |
en |
dc.type |
Journal Article |
en |
dc.identifier.doi |
10.1117/1.1582468 |
en |
pubs.issue |
3 |
en |
pubs.begin-page |
418 |
en |
pubs.volume |
8 |
en |
dc.rights.holder |
Copyright: 2003 Society of Photo-Optical Instrumentation Engineers. |
en |
dc.identifier.pmid |
12880347 |
en |
pubs.end-page |
427 |
en |
dc.rights.accessrights |
http://purl.org/eprint/accessRights/OpenAccess |
en |
pubs.subtype |
Article |
en |
pubs.elements-id |
6215 |
en |
pubs.org-id |
Bioengineering Institute |
en |
pubs.org-id |
ABI Associates |
en |
pubs.org-id |
Medical and Health Sciences |
en |
pubs.org-id |
Medical Sciences |
en |
pubs.org-id |
Science |
en |
pubs.org-id |
Science Research |
en |
pubs.org-id |
Maurice Wilkins Centre (2010-2014) |
en |
pubs.record-created-at-source-date |
2010-09-01 |
en |
pubs.dimensions-id |
12880347 |
en |