@inbook{b52bc1ad555d4ad1ac708023dddebd2a,
title = "Photoactivated localization microscopy for cellular imaging",
abstract = "In a method termed photoactivated localization microscopy (PALM), super-resolution fluorescence imaging can be achieved through the localization of single molecules. This allows the resolution of specific proteins fused to the appropriate fluorescent protein label. Here, we summarize fluorescent proteins suitable for PALM, the technical aspects of multicolor and three-dimensional imaging, and the software packages that are available. Additionally, we highlight several biological applications with an emphasis on neuroscience.",
keywords = "Data analysis for PALM, Fluorescence proteins, Live imaging, Super-resolution microscopy",
author = "Paulina Achurra and Seamus Holden and Thomas Pengo and Suliana Manley",
year = "2014",
doi = "10.1007/978-1-62703-983-3_5",
language = "English (US)",
isbn = "9781627039826",
series = "Neuromethods",
publisher = "Humana Press Inc.",
pages = "87--111",
booktitle = "Super-Resolution Microscopy Techniques in the Neurosciences",
}