Serveur d'exploration sur l'opéra

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

A high-throughput confocal fluorescence microscopy platform to study DNA replication stress in yeast cells.

Identifieur interne : 000243 ( Main/Exploration ); précédent : 000242; suivant : 000244

A high-throughput confocal fluorescence microscopy platform to study DNA replication stress in yeast cells.

Auteurs : Nikko P. Torres [Canada] ; Grant W. Brown

Source :

RBID : pubmed:25916702

English descriptors

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...)


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 

Wicri

This area was generated with Dilib version V0.6.21.
Data generation: Thu Apr 14 14:59:05 2016. Site generation: Thu Jan 4 23:09:23 2024