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@INBOOK{DeNardo:164601,
author = {Stutz, Andrea and Horvath, Gabor L. and Monks, Brian G. and
Latz, Eicke},
editor = {De Nardo, Christine M. and Latz, Eicke},
title = {{ASC} {S}peck {F}ormation as a {R}eadout for {I}nflammasome
{A}ctivation},
volume = {1040},
address = {Totowa, NJ},
publisher = {Humana Press},
reportid = {DZNE-2022-01144},
isbn = {978-1-62703-522-4 (print)},
series = {Methods in Molecular Biology},
pages = {91 - 101},
year = {2013},
comment = {The Inflammasome / De Nardo, Christine M. (Editor) ;
Totowa, NJ : Humana Press, 2013, Chapter 8 ; ISSN:
1064-3745=1940-6029 ; ISBN:
978-1-62703-522-4=978-1-62703-523-1 ;
doi:10.1007/978-1-62703-523-1},
booktitle = {The Inflammasome / De Nardo, Christine
M. (Editor) ; Totowa, NJ : Humana
Press, 2013, Chapter 8 ; ISSN:
1064-3745=1940-6029 ; ISBN:
978-1-62703-522-4=978-1-62703-523-1 ;
doi:10.1007/978-1-62703-523-1},
abstract = {All inflammasomes require the adapter protein apoptosis
associated speck-like protein containing a CARD (ASC) for
the activation of caspase-1. After inflammasome activation,
ASC assembles into a large protein complex, which is termed
'speck'. ASC specks can be observed as they reach a size of
around 1 μm and in most cells only one speck forms upon
inflammasome activation. Hence, ASC speck formation can be
used as a simple upstream readout for inflammasome
activation. Here, we describe a method for analyzing
inflammasome activation by ASC speck visualization. First,
we describe the generation of a clonal inflammasome reporter
macrophage cell line overexpressing fluorescently tagged
ASC. We then discuss stimulation conditions and the
microscopic evaluation of ASC speck formation.},
cin = {AG Latz},
ddc = {570},
cid = {I:(DE-2719)1013024},
pnm = {899 - ohne Topic (POF4-899)},
pid = {G:(DE-HGF)POF4-899},
typ = {PUB:(DE-HGF)7},
pubmed = {pmid:23852599},
doi = {10.1007/978-1-62703-523-1_8},
url = {https://pub.dzne.de/record/164601},
}