Dual fluorescent protein reporters for studying cell behaviors in vivo

HeLa cells transfected with plasmids expressing dual fluorescent protein reporters with cherry, green, and cyan fluorscent proteins. Histone 2B fusions localize fluorescent proteins to the nucleus, while fluorescent proteins fused to glycosylphosphatidylinositol anchor signal sequence localizes to p...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Genesis (New York, N.Y. : 2000) N.Y. : 2000), 2009-10, Vol.47 (10), p.spcone-spcone
Hauptverfasser: Stewart, M. David, Jang, Chuan-Wei, Hong, Nicholas W., Austin, Anthony P., Behringer, Richard R.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page spcone
container_issue 10
container_start_page spcone
container_title Genesis (New York, N.Y. : 2000)
container_volume 47
creator Stewart, M. David
Jang, Chuan-Wei
Hong, Nicholas W.
Austin, Anthony P.
Behringer, Richard R.
description HeLa cells transfected with plasmids expressing dual fluorescent protein reporters with cherry, green, and cyan fluorscent proteins. Histone 2B fusions localize fluorescent proteins to the nucleus, while fluorescent proteins fused to glycosylphosphatidylinositol anchor signal sequence localizes to plasma membranes. These dual fluorescent reporters label nuclear and plasma membranes of live cells to follow their behaviors in developing embryos. See the paper by Stewart et al. in this issue.
doi_str_mv 10.1002/dvg.20582
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_754551354</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>754551354</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2112-e68ddb58a4e97f74f36737c5774d74b14cb09d411ffd765176e64d7dff10c13f3</originalsourceid><addsrcrecordid>eNqFkM1OwzAQhC0EEqVw4A1yQxzS-t_pEbW0IEXlQKEVFyuJ7RJI42Ingb49CQVuiNOuNN-sZgeAcwQHCEI8VM16gCGL8AHoIYZ5OOLR6vBnZ3R1DE68f4GwY3APTCd1UgSmqK3TPtNlFWydrXReBk5vrau084GxLvBVrXZ5uQ4yXRRBqp-TJret1oJN3thTcGSSwuuz79kHD9PrxfgmjO9mt-OrOMwwQjjUPFIqZVFC9UgYQQ3hgoiMCUGVoCmiWQpHiiJkjBKcIcE1bxVlDIIZIob0wcX-bpvyrda-kpvcd5GSUtvaS8EoY4gw-j9JKceYINSSl3syc9Z7p43cunyTuJ1EUHalyrZU-VVqyw737Hte6N3foJw8zn4c4d6R-0p__DoS9yq735lczmdyHpGn-3ixlDH5BKLyiEY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>744622311</pqid></control><display><type>article</type><title>Dual fluorescent protein reporters for studying cell behaviors in vivo</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Stewart, M. David ; Jang, Chuan-Wei ; Hong, Nicholas W. ; Austin, Anthony P. ; Behringer, Richard R.</creator><creatorcontrib>Stewart, M. David ; Jang, Chuan-Wei ; Hong, Nicholas W. ; Austin, Anthony P. ; Behringer, Richard R.</creatorcontrib><description>HeLa cells transfected with plasmids expressing dual fluorescent protein reporters with cherry, green, and cyan fluorscent proteins. Histone 2B fusions localize fluorescent proteins to the nucleus, while fluorescent proteins fused to glycosylphosphatidylinositol anchor signal sequence localizes to plasma membranes. These dual fluorescent reporters label nuclear and plasma membranes of live cells to follow their behaviors in developing embryos. See the paper by Stewart et al. in this issue.</description><identifier>ISSN: 1526-954X</identifier><identifier>EISSN: 1526-968X</identifier><identifier>DOI: 10.1002/dvg.20582</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Prunus</subject><ispartof>Genesis (New York, N.Y. : 2000), 2009-10, Vol.47 (10), p.spcone-spcone</ispartof><rights>Copyright © 2009 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fdvg.20582$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fdvg.20582$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27907,27908,45557,45558</link.rule.ids></links><search><creatorcontrib>Stewart, M. David</creatorcontrib><creatorcontrib>Jang, Chuan-Wei</creatorcontrib><creatorcontrib>Hong, Nicholas W.</creatorcontrib><creatorcontrib>Austin, Anthony P.</creatorcontrib><creatorcontrib>Behringer, Richard R.</creatorcontrib><title>Dual fluorescent protein reporters for studying cell behaviors in vivo</title><title>Genesis (New York, N.Y. : 2000)</title><addtitle>Genesis</addtitle><description>HeLa cells transfected with plasmids expressing dual fluorescent protein reporters with cherry, green, and cyan fluorscent proteins. Histone 2B fusions localize fluorescent proteins to the nucleus, while fluorescent proteins fused to glycosylphosphatidylinositol anchor signal sequence localizes to plasma membranes. These dual fluorescent reporters label nuclear and plasma membranes of live cells to follow their behaviors in developing embryos. See the paper by Stewart et al. in this issue.</description><subject>Prunus</subject><issn>1526-954X</issn><issn>1526-968X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkM1OwzAQhC0EEqVw4A1yQxzS-t_pEbW0IEXlQKEVFyuJ7RJI42Ingb49CQVuiNOuNN-sZgeAcwQHCEI8VM16gCGL8AHoIYZ5OOLR6vBnZ3R1DE68f4GwY3APTCd1UgSmqK3TPtNlFWydrXReBk5vrau084GxLvBVrXZ5uQ4yXRRBqp-TJret1oJN3thTcGSSwuuz79kHD9PrxfgmjO9mt-OrOMwwQjjUPFIqZVFC9UgYQQ3hgoiMCUGVoCmiWQpHiiJkjBKcIcE1bxVlDIIZIob0wcX-bpvyrda-kpvcd5GSUtvaS8EoY4gw-j9JKceYINSSl3syc9Z7p43cunyTuJ1EUHalyrZU-VVqyw737Hte6N3foJw8zn4c4d6R-0p__DoS9yq735lczmdyHpGn-3ixlDH5BKLyiEY</recordid><startdate>200910</startdate><enddate>200910</enddate><creator>Stewart, M. David</creator><creator>Jang, Chuan-Wei</creator><creator>Hong, Nicholas W.</creator><creator>Austin, Anthony P.</creator><creator>Behringer, Richard R.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>200910</creationdate><title>Dual fluorescent protein reporters for studying cell behaviors in vivo</title><author>Stewart, M. David ; Jang, Chuan-Wei ; Hong, Nicholas W. ; Austin, Anthony P. ; Behringer, Richard R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2112-e68ddb58a4e97f74f36737c5774d74b14cb09d411ffd765176e64d7dff10c13f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Prunus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stewart, M. David</creatorcontrib><creatorcontrib>Jang, Chuan-Wei</creatorcontrib><creatorcontrib>Hong, Nicholas W.</creatorcontrib><creatorcontrib>Austin, Anthony P.</creatorcontrib><creatorcontrib>Behringer, Richard R.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Genesis (New York, N.Y. : 2000)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stewart, M. David</au><au>Jang, Chuan-Wei</au><au>Hong, Nicholas W.</au><au>Austin, Anthony P.</au><au>Behringer, Richard R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dual fluorescent protein reporters for studying cell behaviors in vivo</atitle><jtitle>Genesis (New York, N.Y. : 2000)</jtitle><addtitle>Genesis</addtitle><date>2009-10</date><risdate>2009</risdate><volume>47</volume><issue>10</issue><spage>spcone</spage><epage>spcone</epage><pages>spcone-spcone</pages><issn>1526-954X</issn><eissn>1526-968X</eissn><abstract>HeLa cells transfected with plasmids expressing dual fluorescent protein reporters with cherry, green, and cyan fluorscent proteins. Histone 2B fusions localize fluorescent proteins to the nucleus, while fluorescent proteins fused to glycosylphosphatidylinositol anchor signal sequence localizes to plasma membranes. These dual fluorescent reporters label nuclear and plasma membranes of live cells to follow their behaviors in developing embryos. See the paper by Stewart et al. in this issue.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/dvg.20582</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1526-954X
ispartof Genesis (New York, N.Y. : 2000), 2009-10, Vol.47 (10), p.spcone-spcone
issn 1526-954X
1526-968X
language eng
recordid cdi_proquest_miscellaneous_754551354
source Wiley Online Library Journals Frontfile Complete
subjects Prunus
title Dual fluorescent protein reporters for studying cell behaviors in vivo
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T11%3A43%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Dual%20fluorescent%20protein%20reporters%20for%20studying%20cell%20behaviors%20in%20vivo&rft.jtitle=Genesis%20(New%20York,%20N.Y.%20:%202000)&rft.au=Stewart,%20M.%20David&rft.date=2009-10&rft.volume=47&rft.issue=10&rft.spage=spcone&rft.epage=spcone&rft.pages=spcone-spcone&rft.issn=1526-954X&rft.eissn=1526-968X&rft_id=info:doi/10.1002/dvg.20582&rft_dat=%3Cproquest_cross%3E754551354%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=744622311&rft_id=info:pmid/&rfr_iscdi=true