Simultaneous demonstration of microfilaments and intermediate-sized filaments in the lens by double immunofluorescence

Actin- and vimentin filaments (microfilaments and intermediate-sized filaments) are the major components of the lens fiber cytoskeleton. Indirect immunofluorescence suggests a quite different localization of the two kinds of filamentous structures. Actin can only be visualized along the fiber plasma...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Experimental eye research 1982-10, Vol.35 (4), p.363-369
Hauptverfasser: Ramaekers, F.C.S., Poels, L.G., Jap, P.H.K., Bloemendal, H.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 369
container_issue 4
container_start_page 363
container_title Experimental eye research
container_volume 35
creator Ramaekers, F.C.S.
Poels, L.G.
Jap, P.H.K.
Bloemendal, H.
description Actin- and vimentin filaments (microfilaments and intermediate-sized filaments) are the major components of the lens fiber cytoskeleton. Indirect immunofluorescence suggests a quite different localization of the two kinds of filamentous structures. Actin can only be visualized along the fiber plasma membrane, while vimentin-containing elements seem to fill up the cytoplasmic space. The results are independent of the sequence of staining.
doi_str_mv 10.1016/0014-4835(82)90099-9
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_74200233</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0014483582900999</els_id><sourcerecordid>74200233</sourcerecordid><originalsourceid>FETCH-LOGICAL-c357t-6cc1a8de97012232b0ddbe608574927dd11e56984d1c18617680f2ca4c413f253</originalsourceid><addsrcrecordid>eNp9kF1rFTEQhoMo9bT6DxRyJfZi7eRjN5sboRS_oNCL6nXIJrMY2SQ1yRbaX-8ez6HeeTUw874z8z6EvGHwgQEbLgCY7OQo-vcjP9cAWnf6Gdkx0EMHAOo52T1JXpLTWn9tXSGVPCEng-qlBLEj97chrkuzCfNaqceYU23FtpATzTONwZU8h8VGTK1SmzwNqWGJ6INt2NXwiJ7-E4RE20-kC6ZKpwfq8zotSEOMa8rzsuaC1WFy-Iq8mO1S8fWxnpEfnz99v_raXd98-XZ1ed050avWDc4xO3rUChjngk_g_YQDjL2SmivvGcN-0KP0zLFxYGoYYebOSieZmHkvzsi7w967kn-vWJuJYftgWQ6BjZIcgAuxCeVBuOWtteBs7kqItjwYBmaP2-xZmj1LM3LzF7fRm-3tcf86bUyeTEe-2_zjYY5byPuAxVQX9gB8KOia8Tn8_8Af43iRHA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>74200233</pqid></control><display><type>article</type><title>Simultaneous demonstration of microfilaments and intermediate-sized filaments in the lens by double immunofluorescence</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Ramaekers, F.C.S. ; Poels, L.G. ; Jap, P.H.K. ; Bloemendal, H.</creator><creatorcontrib>Ramaekers, F.C.S. ; Poels, L.G. ; Jap, P.H.K. ; Bloemendal, H.</creatorcontrib><description>Actin- and vimentin filaments (microfilaments and intermediate-sized filaments) are the major components of the lens fiber cytoskeleton. Indirect immunofluorescence suggests a quite different localization of the two kinds of filamentous structures. Actin can only be visualized along the fiber plasma membrane, while vimentin-containing elements seem to fill up the cytoplasmic space. The results are independent of the sequence of staining.</description><identifier>ISSN: 0014-4835</identifier><identifier>EISSN: 1096-0007</identifier><identifier>DOI: 10.1016/0014-4835(82)90099-9</identifier><identifier>PMID: 6754403</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Actins - analysis ; Animals ; Cattle ; Cytoskeleton - analysis ; Electrophoresis ; Fluorescent Antibody Technique ; Immune Sera - immunology ; Intermediate Filament Proteins - analysis ; Lens, Crystalline - ultrastructure ; Vimentin</subject><ispartof>Experimental eye research, 1982-10, Vol.35 (4), p.363-369</ispartof><rights>1982</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-6cc1a8de97012232b0ddbe608574927dd11e56984d1c18617680f2ca4c413f253</citedby><cites>FETCH-LOGICAL-c357t-6cc1a8de97012232b0ddbe608574927dd11e56984d1c18617680f2ca4c413f253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/0014483582900999$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6754403$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ramaekers, F.C.S.</creatorcontrib><creatorcontrib>Poels, L.G.</creatorcontrib><creatorcontrib>Jap, P.H.K.</creatorcontrib><creatorcontrib>Bloemendal, H.</creatorcontrib><title>Simultaneous demonstration of microfilaments and intermediate-sized filaments in the lens by double immunofluorescence</title><title>Experimental eye research</title><addtitle>Exp Eye Res</addtitle><description>Actin- and vimentin filaments (microfilaments and intermediate-sized filaments) are the major components of the lens fiber cytoskeleton. Indirect immunofluorescence suggests a quite different localization of the two kinds of filamentous structures. Actin can only be visualized along the fiber plasma membrane, while vimentin-containing elements seem to fill up the cytoplasmic space. The results are independent of the sequence of staining.</description><subject>Actins - analysis</subject><subject>Animals</subject><subject>Cattle</subject><subject>Cytoskeleton - analysis</subject><subject>Electrophoresis</subject><subject>Fluorescent Antibody Technique</subject><subject>Immune Sera - immunology</subject><subject>Intermediate Filament Proteins - analysis</subject><subject>Lens, Crystalline - ultrastructure</subject><subject>Vimentin</subject><issn>0014-4835</issn><issn>1096-0007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF1rFTEQhoMo9bT6DxRyJfZi7eRjN5sboRS_oNCL6nXIJrMY2SQ1yRbaX-8ez6HeeTUw874z8z6EvGHwgQEbLgCY7OQo-vcjP9cAWnf6Gdkx0EMHAOo52T1JXpLTWn9tXSGVPCEng-qlBLEj97chrkuzCfNaqceYU23FtpATzTONwZU8h8VGTK1SmzwNqWGJ6INt2NXwiJ7-E4RE20-kC6ZKpwfq8zotSEOMa8rzsuaC1WFy-Iq8mO1S8fWxnpEfnz99v_raXd98-XZ1ed050avWDc4xO3rUChjngk_g_YQDjL2SmivvGcN-0KP0zLFxYGoYYebOSieZmHkvzsi7w967kn-vWJuJYftgWQ6BjZIcgAuxCeVBuOWtteBs7kqItjwYBmaP2-xZmj1LM3LzF7fRm-3tcf86bUyeTEe-2_zjYY5byPuAxVQX9gB8KOia8Tn8_8Af43iRHA</recordid><startdate>198210</startdate><enddate>198210</enddate><creator>Ramaekers, F.C.S.</creator><creator>Poels, L.G.</creator><creator>Jap, P.H.K.</creator><creator>Bloemendal, H.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>198210</creationdate><title>Simultaneous demonstration of microfilaments and intermediate-sized filaments in the lens by double immunofluorescence</title><author>Ramaekers, F.C.S. ; Poels, L.G. ; Jap, P.H.K. ; Bloemendal, H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-6cc1a8de97012232b0ddbe608574927dd11e56984d1c18617680f2ca4c413f253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>Actins - analysis</topic><topic>Animals</topic><topic>Cattle</topic><topic>Cytoskeleton - analysis</topic><topic>Electrophoresis</topic><topic>Fluorescent Antibody Technique</topic><topic>Immune Sera - immunology</topic><topic>Intermediate Filament Proteins - analysis</topic><topic>Lens, Crystalline - ultrastructure</topic><topic>Vimentin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramaekers, F.C.S.</creatorcontrib><creatorcontrib>Poels, L.G.</creatorcontrib><creatorcontrib>Jap, P.H.K.</creatorcontrib><creatorcontrib>Bloemendal, H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental eye research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramaekers, F.C.S.</au><au>Poels, L.G.</au><au>Jap, P.H.K.</au><au>Bloemendal, H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous demonstration of microfilaments and intermediate-sized filaments in the lens by double immunofluorescence</atitle><jtitle>Experimental eye research</jtitle><addtitle>Exp Eye Res</addtitle><date>1982-10</date><risdate>1982</risdate><volume>35</volume><issue>4</issue><spage>363</spage><epage>369</epage><pages>363-369</pages><issn>0014-4835</issn><eissn>1096-0007</eissn><abstract>Actin- and vimentin filaments (microfilaments and intermediate-sized filaments) are the major components of the lens fiber cytoskeleton. Indirect immunofluorescence suggests a quite different localization of the two kinds of filamentous structures. Actin can only be visualized along the fiber plasma membrane, while vimentin-containing elements seem to fill up the cytoplasmic space. The results are independent of the sequence of staining.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>6754403</pmid><doi>10.1016/0014-4835(82)90099-9</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0014-4835
ispartof Experimental eye research, 1982-10, Vol.35 (4), p.363-369
issn 0014-4835
1096-0007
language eng
recordid cdi_proquest_miscellaneous_74200233
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Actins - analysis
Animals
Cattle
Cytoskeleton - analysis
Electrophoresis
Fluorescent Antibody Technique
Immune Sera - immunology
Intermediate Filament Proteins - analysis
Lens, Crystalline - ultrastructure
Vimentin
title Simultaneous demonstration of microfilaments and intermediate-sized filaments in the lens by double immunofluorescence
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-19T18%3A58%3A49IST&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=Simultaneous%20demonstration%20of%20microfilaments%20and%20intermediate-sized%20filaments%20in%20the%20lens%20by%20double%20immunofluorescence&rft.jtitle=Experimental%20eye%20research&rft.au=Ramaekers,%20F.C.S.&rft.date=1982-10&rft.volume=35&rft.issue=4&rft.spage=363&rft.epage=369&rft.pages=363-369&rft.issn=0014-4835&rft.eissn=1096-0007&rft_id=info:doi/10.1016/0014-4835(82)90099-9&rft_dat=%3Cproquest_cross%3E74200233%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=74200233&rft_id=info:pmid/6754403&rft_els_id=0014483582900999&rfr_iscdi=true