A high-throughput confocal fluorescence microscopy platform to study DNA replication stress in yeast cells.
Identifieur interne : 000243 ( Main/Exploration ); précédent : 000242; suivant : 000244A high-throughput confocal fluorescence microscopy platform to study DNA replication stress in yeast cells.
Auteurs : Nikko P. Torres [Canada] ; Grant W. BrownSource :
- Methods in molecular biology (Clifton, N.J.) ; 2015.
English descriptors
- KwdEn :
- MESH :
- cytology : Saccharomyces cerevisiae.
- growth & development : Saccharomyces cerevisiae.
- metabolism : Saccharomyces cerevisiae.
- methods : Microscopy, Confocal, Microscopy, Fluorescence.
- Cells, Cultured, DNA Replication, Imaging, Three-Dimensional, Stress, Physiological, Time Factors.
Abstract
High-throughput imaging of yeast cells expressing fluorescent proteins can be used to understand biological pathways in the context of spatial organization. Here we describe a method for imaging yeast cells expressing proteins tagged with green fluorescent protein (GFP) and/or red fluorescent protein (RFP), with or without drug treatment, in a 384-well format, using the PerkinElmer Opera high-content confocal imaging microscope.
DOI: 10.1007/978-1-4939-2596-4_1
PubMed: 25916702
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000084
- to stream PubMed, to step Curation: 000084
- to stream PubMed, to step Checkpoint: 000128
- to stream Ncbi, to step Merge: 000D46
- to stream Ncbi, to step Curation: 000D46
- to stream Ncbi, to step Checkpoint: 000D46
- to stream Main, to step Merge: 000240
- to stream Main, to step Curation: 000243
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">A high-throughput confocal fluorescence microscopy platform to study DNA replication stress in yeast cells.</title>
<author><name sortKey="Torres, Nikko P" sort="Torres, Nikko P" uniqKey="Torres N" first="Nikko P" last="Torres">Nikko P. Torres</name>
<affiliation wicri:level="4"><nlm:affiliation>Department of Biochemistry and Donnelly Centre, University of Toronto, 160 College Street, Toronto, ON, Canada, M5S 3E1.</nlm:affiliation>
<orgName type="university">Université de Toronto</orgName>
<country>Canada</country>
<placeName><settlement type="city">Toronto</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Brown, Grant W" sort="Brown, Grant W" uniqKey="Brown G" first="Grant W" last="Brown">Grant W. Brown</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="2015">2015</date>
<idno type="doi">10.1007/978-1-4939-2596-4_1</idno>
<idno type="RBID">pubmed:25916702</idno>
<idno type="pmid">25916702</idno>
<idno type="wicri:Area/PubMed/Corpus">000084</idno>
<idno type="wicri:Area/PubMed/Curation">000084</idno>
<idno type="wicri:Area/PubMed/Checkpoint">000128</idno>
<idno type="wicri:Area/Ncbi/Merge">000D46</idno>
<idno type="wicri:Area/Ncbi/Curation">000D46</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">000D46</idno>
<idno type="wicri:Area/Main/Merge">000240</idno>
<idno type="wicri:Area/Main/Curation">000243</idno>
<idno type="wicri:Area/Main/Exploration">000243</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">A high-throughput confocal fluorescence microscopy platform to study DNA replication stress in yeast cells.</title>
<author><name sortKey="Torres, Nikko P" sort="Torres, Nikko P" uniqKey="Torres N" first="Nikko P" last="Torres">Nikko P. Torres</name>
<affiliation wicri:level="4"><nlm:affiliation>Department of Biochemistry and Donnelly Centre, University of Toronto, 160 College Street, Toronto, ON, Canada, M5S 3E1.</nlm:affiliation>
<orgName type="university">Université de Toronto</orgName>
<country>Canada</country>
<placeName><settlement type="city">Toronto</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Brown, Grant W" sort="Brown, Grant W" uniqKey="Brown G" first="Grant W" last="Brown">Grant W. Brown</name>
</author>
</analytic>
<series><title level="j">Methods in molecular biology (Clifton, N.J.)</title>
<idno type="e-ISSN">1940-6029</idno>
<imprint><date when="2015" type="published">2015</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cells, Cultured</term>
<term>DNA Replication</term>
<term>Imaging, Three-Dimensional</term>
<term>Microscopy, Confocal (methods)</term>
<term>Microscopy, Fluorescence (methods)</term>
<term>Saccharomyces cerevisiae (cytology)</term>
<term>Saccharomyces cerevisiae (growth & development)</term>
<term>Saccharomyces cerevisiae (metabolism)</term>
<term>Stress, Physiological</term>
<term>Time Factors</term>
</keywords>
<keywords scheme="MESH" qualifier="cytology" xml:lang="en"><term>Saccharomyces cerevisiae</term>
</keywords>
<keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Saccharomyces cerevisiae</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Saccharomyces cerevisiae</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Microscopy, Confocal</term>
<term>Microscopy, Fluorescence</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Cells, Cultured</term>
<term>DNA Replication</term>
<term>Imaging, Three-Dimensional</term>
<term>Stress, Physiological</term>
<term>Time Factors</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">High-throughput imaging of yeast cells expressing fluorescent proteins can be used to understand biological pathways in the context of spatial organization. Here we describe a method for imaging yeast cells expressing proteins tagged with green fluorescent protein (GFP) and/or red fluorescent protein (RFP), with or without drug treatment, in a 384-well format, using the PerkinElmer Opera high-content confocal imaging microscope.</div>
</front>
</TEI>
<affiliations><list><country><li>Canada</li>
</country>
<region><li>Ontario</li>
</region>
<settlement><li>Toronto</li>
</settlement>
<orgName><li>Université de Toronto</li>
</orgName>
</list>
<tree><noCountry><name sortKey="Brown, Grant W" sort="Brown, Grant W" uniqKey="Brown G" first="Grant W" last="Brown">Grant W. Brown</name>
</noCountry>
<country name="Canada"><region name="Ontario"><name sortKey="Torres, Nikko P" sort="Torres, Nikko P" uniqKey="Torres N" first="Nikko P" last="Torres">Nikko P. Torres</name>
</region>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Musique/explor/OperaV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000243 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000243 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Musique |area= OperaV1 |flux= Main |étape= Exploration |type= RBID |clé= pubmed:25916702 |texte= A high-throughput confocal fluorescence microscopy platform to study DNA replication stress in yeast cells. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:25916702" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \ | NlmPubMed2Wicri -a OperaV1
This area was generated with Dilib version V0.6.21. |