NDLI: Super-resolution binding activated localization microscopy through reversible change of DNA conformation

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Super-resolution binding activated localization microscopy through reversible change of DNA conformation

Content Provider	Scilit
Author	Szczurek, Aleksander Birk, Udo Knecht, Hans Dobrucki, Jerzy Mai, Sabine Cremer, Christoph
Copyright Year	2018
Description	Methods of super-resolving light microscopy (SRM) have found an exponentially growing range of applications in cell biology, including nuclear structure analyses. Recent developments have proven that Single Molecule Localization Microscopy (SMLM), a type of SRM, is particularly useful for enhanced spatial analysis of the cell nucleus due to its highest resolving capability combined with very specific fluorescent labeling. In this commentary we offer a brief review of the latest methodological development in the field of SMLM of chromatin designated DNA Structure Fluctuation Assisted Binding Activated Localization Microscopy (abbreviated as fBALM) as well as its potential future applications in biology and medicine.
Related Links	https://www.tandfonline.com/doi/pdf/10.1080/19491034.2017.1419846?needAccess=true https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973136/pdf
Ending Page	189
Page Count	8
Starting Page	182
ISSN	19491034
e-ISSN	19491042
DOI	10.1080/19491034.2017.1419846
Journal	Nucleus
Issue Number	1
Volume Number	9
Language	English
Publisher	Informa UK Limited
Publisher Date	2018-12-31
Access Restriction	Open
Subject Keyword	Journal: Nucleus Microscopic Research Chromatin Dna Fbalm, Smlm Nucleus Single Molecule Localization Super-resolution Microscopy
Content Type	Text
Resource Type	Article
Subject	Cell Biology Medicine

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