DNA CONTENT OF PURIFIED PREPARATIONS OF MOUSE PURKINJE NEURONS ISOLATED BY A VELOCITY SEDIMENTATION TECHNIQUE

— The DNA content of mouse Purkinje neurons was investigated employing a biochemical approach. Material for the biochemical assay was provided by means of a sedimentation velocity separation technique which yields bulk quantities of well‐preserved Purkinje perikarya in a high degree of purity. The s...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of neurochemistry 1973-03, Vol.20 (3), p.651-657
Hauptverfasser: Cohen, J., Mareš, V., Lodin, Z.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 657
container_issue 3
container_start_page 651
container_title Journal of neurochemistry
container_volume 20
creator Cohen, J.
Mareš, V.
Lodin, Z.
description — The DNA content of mouse Purkinje neurons was investigated employing a biochemical approach. Material for the biochemical assay was provided by means of a sedimentation velocity separation technique which yields bulk quantities of well‐preserved Purkinje perikarya in a high degree of purity. The same amount of DNA/cell was recorded for mixed cerebellar cell somata (7·6 ± 0±2 pg/cell), as for the Purkinje perikarya enriched fractions (7±2 & 0·2 pg/cell). No evidence could be found for the existence of a tetraploid DNA complement in mouse Purkinje neurons despite indications to the contrary from a parallel cytophotometric study.
doi_str_mv 10.1111/j.1471-4159.1973.tb00025.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_81900613</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>81900613</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3691-4211aece271710380479710dd83cc1c5b475c51f3368913e5425fc31fafb98b93</originalsourceid><addsrcrecordid>eNqVkEFv2jAYhq1qVcu6_oRK1g67kfmL7STuYVIazHBHEwZJJU5WYhwJBKVLQIN_P6cg7vPFlp_3e209CH0F4oFb31cesBD6DLjwQITU21WEEJ97hyvUu6BPqOcu_T4lzL9Fn9t2RQgELIAbdMN4yEBAD20GaYyTLM1lmuNsiCfFVA2VHODJVE7iaZyrLJ114CUrZrLDv1T6LHEqi2lH1Cwbx7nLP81xjF_lOEtUPsczOVAvrvJjHucyGaXqdyG_oOu6XLf2_rzfoWIo82TUH2c_VRKP-4YGwv3eByitsX4IIRAaERYKd1gsImoMGF6xkBsONaVBJIBaznxeGwp1WVciqgS9Q99Ove_N9s_etju9WbbGrtflm93uWx2BICQA6oKPp6Bptm3b2Fq_N8tN2Rw1EN251ivdCdWdUN251mfX-uCGH86v7KuNXVxGz3Id_3Hif5dre_yPZv2cJgEH-g-CRoRp</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>81900613</pqid></control><display><type>article</type><title>DNA CONTENT OF PURIFIED PREPARATIONS OF MOUSE PURKINJE NEURONS ISOLATED BY A VELOCITY SEDIMENTATION TECHNIQUE</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Cohen, J. ; Mareš, V. ; Lodin, Z.</creator><creatorcontrib>Cohen, J. ; Mareš, V. ; Lodin, Z.</creatorcontrib><description>— The DNA content of mouse Purkinje neurons was investigated employing a biochemical approach. Material for the biochemical assay was provided by means of a sedimentation velocity separation technique which yields bulk quantities of well‐preserved Purkinje perikarya in a high degree of purity. The same amount of DNA/cell was recorded for mixed cerebellar cell somata (7·6 ± 0±2 pg/cell), as for the Purkinje perikarya enriched fractions (7±2 &amp; 0·2 pg/cell). No evidence could be found for the existence of a tetraploid DNA complement in mouse Purkinje neurons despite indications to the contrary from a parallel cytophotometric study.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/j.1471-4159.1973.tb00025.x</identifier><identifier>PMID: 4574191</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Cell Nucleus - analysis ; Cerebellum - analysis ; Cerebellum - cytology ; Cytological Techniques ; DNA - analysis ; Female ; Histocytochemistry ; Male ; Mice ; Mice, Inbred Strains ; Microscopy, Phase-Contrast ; Purkinje Cells - analysis</subject><ispartof>Journal of neurochemistry, 1973-03, Vol.20 (3), p.651-657</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3691-4211aece271710380479710dd83cc1c5b475c51f3368913e5425fc31fafb98b93</citedby><cites>FETCH-LOGICAL-c3691-4211aece271710380479710dd83cc1c5b475c51f3368913e5425fc31fafb98b93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1471-4159.1973.tb00025.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1471-4159.1973.tb00025.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4574191$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cohen, J.</creatorcontrib><creatorcontrib>Mareš, V.</creatorcontrib><creatorcontrib>Lodin, Z.</creatorcontrib><title>DNA CONTENT OF PURIFIED PREPARATIONS OF MOUSE PURKINJE NEURONS ISOLATED BY A VELOCITY SEDIMENTATION TECHNIQUE</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>— The DNA content of mouse Purkinje neurons was investigated employing a biochemical approach. Material for the biochemical assay was provided by means of a sedimentation velocity separation technique which yields bulk quantities of well‐preserved Purkinje perikarya in a high degree of purity. The same amount of DNA/cell was recorded for mixed cerebellar cell somata (7·6 ± 0±2 pg/cell), as for the Purkinje perikarya enriched fractions (7±2 &amp; 0·2 pg/cell). No evidence could be found for the existence of a tetraploid DNA complement in mouse Purkinje neurons despite indications to the contrary from a parallel cytophotometric study.</description><subject>Animals</subject><subject>Cell Nucleus - analysis</subject><subject>Cerebellum - analysis</subject><subject>Cerebellum - cytology</subject><subject>Cytological Techniques</subject><subject>DNA - analysis</subject><subject>Female</subject><subject>Histocytochemistry</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Microscopy, Phase-Contrast</subject><subject>Purkinje Cells - analysis</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1973</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkEFv2jAYhq1qVcu6_oRK1g67kfmL7STuYVIazHBHEwZJJU5WYhwJBKVLQIN_P6cg7vPFlp_3e209CH0F4oFb31cesBD6DLjwQITU21WEEJ97hyvUu6BPqOcu_T4lzL9Fn9t2RQgELIAbdMN4yEBAD20GaYyTLM1lmuNsiCfFVA2VHODJVE7iaZyrLJ114CUrZrLDv1T6LHEqi2lH1Cwbx7nLP81xjF_lOEtUPsczOVAvrvJjHucyGaXqdyG_oOu6XLf2_rzfoWIo82TUH2c_VRKP-4YGwv3eByitsX4IIRAaERYKd1gsImoMGF6xkBsONaVBJIBaznxeGwp1WVciqgS9Q99Ove_N9s_etju9WbbGrtflm93uWx2BICQA6oKPp6Bptm3b2Fq_N8tN2Rw1EN251ivdCdWdUN251mfX-uCGH86v7KuNXVxGz3Id_3Hif5dre_yPZv2cJgEH-g-CRoRp</recordid><startdate>197303</startdate><enddate>197303</enddate><creator>Cohen, J.</creator><creator>Mareš, V.</creator><creator>Lodin, Z.</creator><general>Blackwell Publishing 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>197303</creationdate><title>DNA CONTENT OF PURIFIED PREPARATIONS OF MOUSE PURKINJE NEURONS ISOLATED BY A VELOCITY SEDIMENTATION TECHNIQUE</title><author>Cohen, J. ; Mareš, V. ; Lodin, Z.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3691-4211aece271710380479710dd83cc1c5b475c51f3368913e5425fc31fafb98b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1973</creationdate><topic>Animals</topic><topic>Cell Nucleus - analysis</topic><topic>Cerebellum - analysis</topic><topic>Cerebellum - cytology</topic><topic>Cytological Techniques</topic><topic>DNA - analysis</topic><topic>Female</topic><topic>Histocytochemistry</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Microscopy, Phase-Contrast</topic><topic>Purkinje Cells - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cohen, J.</creatorcontrib><creatorcontrib>Mareš, V.</creatorcontrib><creatorcontrib>Lodin, Z.</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>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cohen, J.</au><au>Mareš, V.</au><au>Lodin, Z.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DNA CONTENT OF PURIFIED PREPARATIONS OF MOUSE PURKINJE NEURONS ISOLATED BY A VELOCITY SEDIMENTATION TECHNIQUE</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1973-03</date><risdate>1973</risdate><volume>20</volume><issue>3</issue><spage>651</spage><epage>657</epage><pages>651-657</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><abstract>— The DNA content of mouse Purkinje neurons was investigated employing a biochemical approach. Material for the biochemical assay was provided by means of a sedimentation velocity separation technique which yields bulk quantities of well‐preserved Purkinje perikarya in a high degree of purity. The same amount of DNA/cell was recorded for mixed cerebellar cell somata (7·6 ± 0±2 pg/cell), as for the Purkinje perikarya enriched fractions (7±2 &amp; 0·2 pg/cell). No evidence could be found for the existence of a tetraploid DNA complement in mouse Purkinje neurons despite indications to the contrary from a parallel cytophotometric study.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>4574191</pmid><doi>10.1111/j.1471-4159.1973.tb00025.x</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-3042
ispartof Journal of neurochemistry, 1973-03, Vol.20 (3), p.651-657
issn 0022-3042
1471-4159
language eng
recordid cdi_proquest_miscellaneous_81900613
source MEDLINE; Access via Wiley Online Library
subjects Animals
Cell Nucleus - analysis
Cerebellum - analysis
Cerebellum - cytology
Cytological Techniques
DNA - analysis
Female
Histocytochemistry
Male
Mice
Mice, Inbred Strains
Microscopy, Phase-Contrast
Purkinje Cells - analysis
title DNA CONTENT OF PURIFIED PREPARATIONS OF MOUSE PURKINJE NEURONS ISOLATED BY A VELOCITY SEDIMENTATION TECHNIQUE
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T20%3A58%3A55IST&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=DNA%20CONTENT%20OF%20PURIFIED%20PREPARATIONS%20OF%20MOUSE%20PURKINJE%20NEURONS%20ISOLATED%20BY%20A%20VELOCITY%20SEDIMENTATION%20TECHNIQUE&rft.jtitle=Journal%20of%20neurochemistry&rft.au=Cohen,%20J.&rft.date=1973-03&rft.volume=20&rft.issue=3&rft.spage=651&rft.epage=657&rft.pages=651-657&rft.issn=0022-3042&rft.eissn=1471-4159&rft_id=info:doi/10.1111/j.1471-4159.1973.tb00025.x&rft_dat=%3Cproquest_cross%3E81900613%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=81900613&rft_id=info:pmid/4574191&rfr_iscdi=true