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Journal ArticleDOI

Super-resolution fluorescence imaging of chromosomal DNA.

TLDR
It is demonstrated that robust and detailed super-resolution images of DNA can be produced by combining 5-ethynyl-2'-deoxyuridine (EdU) labeling using the 'click chemistry' approach and direct stochastic optical reconstruction microscopy (dSTORM).
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This article is published in Journal of Structural Biology.The article was published on 2012-02-01. It has received 100 citations till now. The article focuses on the topics: Fluorescence-lifetime imaging microscopy.

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Citations
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ChromEMT: Visualizing 3D chromatin structure and compaction in interphase and mitotic cells

TL;DR: ChromEMT enables the ultrastructure of individual chromatin chains, heterochromatin domains, and mitotic chromosomes to be resolved in serial slices and their 3D organization to be visualized as a continuum through large nuclear volumes in situ.
Journal ArticleDOI

Precisely and accurately localizing single emitters in fluorescence microscopy

TL;DR: A lucid synthesis of the developments on single-molecule localization precision and accuracy and their practical implications are presented in order to guide the increasing number of researchers using single-particle tracking and super-resolution localization microscopy.
Journal ArticleDOI

Single-Molecule Localization Microscopy in Eukaryotes.

TL;DR: How SMLM has contributed new knowledge in eukaryotic biology is described, and the potential to pave the way toward a better understanding of how cells function at the molecular level is described.
Journal ArticleDOI

Single-molecule localization microscopy

TL;DR: This Primer explains the central concepts of single-molecule localization microscopy before discussing experimental considerations regarding fluorophores, optics and data acquisition, processing and analysis, and describes recent high-impact discoveries made by SMLM techniques.
References
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Journal ArticleDOI

Imaging intracellular fluorescent proteins at nanometer resolution.

TL;DR: This work introduced a method for optically imaging intracellular proteins at nanometer spatial resolution and used this method to image specific target proteins in thin sections of lysosomes and mitochondria and in fixed whole cells to image retroviral protein Gag at the plasma membrane.
Journal ArticleDOI

Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM).

TL;DR: A high-resolution fluorescence microscopy method based on high-accuracy localization of photoswitchable fluorophores that can, in principle, reach molecular-scale resolution is developed.
Journal ArticleDOI

A chemical method for fast and sensitive detection of DNA synthesis in vivo

TL;DR: The method does not require sample fixation or DNA denaturation and permits good structural preservation, and the small size of the fluorescent azides used for detection results in a high degree of specimen penetration, allowing the staining of whole-mount preparations of large tissue and organ explants.
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