dc.contributor.author |
Henriques, R
|
|
dc.contributor.author |
Griffiths, C
|
|
dc.contributor.author |
Rego, EH
|
|
dc.contributor.author |
Mhlanga, Musa
|
|
dc.date.accessioned |
2011-12-14T10:34:57Z |
|
dc.date.available |
2011-12-14T10:34:57Z |
|
dc.date.issued |
2011-05 |
|
dc.identifier.citation |
Henriques, R, Griffiths, C et al. 2011. PALM and STORM: unlocking live-cell super-resolution. Biopolymers, Vol 95(5), pp 322-331 |
en_US |
dc.identifier.issn |
0006-3525 |
|
dc.identifier.uri |
http://onlinelibrary.wiley.com/doi/10.1002/bip.21586/abstract
|
|
dc.identifier.uri |
http://hdl.handle.net/10204/5414
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|
dc.description |
Copyright: 2011 Wiley Blackwell. This is an ABSTRACT ONLY |
en_US |
dc.description.abstract |
Live-cell fluorescence light microscopy has emerged as an important tool in the study of cellular biology. The development of fluorescent markers in parallel with super-resolution imaging systems has pushed light microscopy into the realm of molecular visualization at the nanometer scale. Resolutions previously only attained with electron microscopes are now within the grasp of light microscopes. However, until recently, live-cell imaging approaches have eluded super-resolution microscopy, hampering it from reaching its full potential for revealing the dynamic interactions in biology occurring at the single molecule level. Here we examine recent advances in the super-resolution imaging of living cells by reviewing recent breakthroughs in single molecule localization microscopy methods such as PALM and STORM to achieve this important goal. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Wiley Blackwell |
en_US |
dc.relation.ispartofseries |
Workflow request;6582 |
|
dc.subject |
Super-resolution |
en_US |
dc.subject |
Microscopy methods |
en_US |
dc.subject |
Single molecules |
en_US |
dc.subject |
PALM |
en_US |
dc.subject |
STORM |
en_US |
dc.subject |
Live-cell imaging |
en_US |
dc.subject |
Super-resolution microscopy |
en_US |
dc.title |
PALM and STORM: unlocking live-cell super-resolution |
en_US |
dc.type |
Article |
en_US |
dc.identifier.apacitation |
Henriques, R., Griffiths, C., Rego, E., & Mhlanga, M. (2011). PALM and STORM: unlocking live-cell super-resolution. http://hdl.handle.net/10204/5414 |
en_ZA |
dc.identifier.chicagocitation |
Henriques, R, C Griffiths, EH Rego, and Musa Mhlanga "PALM and STORM: unlocking live-cell super-resolution." (2011) http://hdl.handle.net/10204/5414 |
en_ZA |
dc.identifier.vancouvercitation |
Henriques R, Griffiths C, Rego E, Mhlanga M. PALM and STORM: unlocking live-cell super-resolution. 2011; http://hdl.handle.net/10204/5414. |
en_ZA |
dc.identifier.ris |
TY - Article
AU - Henriques, R
AU - Griffiths, C
AU - Rego, EH
AU - Mhlanga, Musa
AB - Live-cell fluorescence light microscopy has emerged as an important tool in the study of cellular biology. The development of fluorescent markers in parallel with super-resolution imaging systems has pushed light microscopy into the realm of molecular visualization at the nanometer scale. Resolutions previously only attained with electron microscopes are now within the grasp of light microscopes. However, until recently, live-cell imaging approaches have eluded super-resolution microscopy, hampering it from reaching its full potential for revealing the dynamic interactions in biology occurring at the single molecule level. Here we examine recent advances in the super-resolution imaging of living cells by reviewing recent breakthroughs in single molecule localization microscopy methods such as PALM and STORM to achieve this important goal.
DA - 2011-05
DB - ResearchSpace
DP - CSIR
KW - Super-resolution
KW - Microscopy methods
KW - Single molecules
KW - PALM
KW - STORM
KW - Live-cell imaging
KW - Super-resolution microscopy
LK - https://researchspace.csir.co.za
PY - 2011
SM - 0006-3525
T1 - PALM and STORM: unlocking live-cell super-resolution
TI - PALM and STORM: unlocking live-cell super-resolution
UR - http://hdl.handle.net/10204/5414
ER -
|
en_ZA |