Comparison of methods for quantification of ribozyme cleavage
Copyright information:Taken from "A structural analysis of catalytic activities of hammerhead ribozymes"http://www.biomedcentral.com/1471-2105/8/469BMC Bioinformatics 2007;8():469-469.Published online 30 Nov 2007PMCID:PMC2238771. Ribozyme GUC7 was incubated for various lengths of time from...
Gespeichert in:
Hauptverfasser: | , , , , , |
---|---|
Format: | Bild |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | |
container_volume | |
creator | Shao, Yu Wu, Susan Chan, Chi Yu Klapper, Jessie R Schneider, Erasmus Ding, Ye |
description | Copyright information:Taken from "A structural analysis of catalytic activities of hammerhead ribozymes"http://www.biomedcentral.com/1471-2105/8/469BMC Bioinformatics 2007;8():469-469.Published online 30 Nov 2007PMCID:PMC2238771. Ribozyme GUC7 was incubated for various lengths of time from 0 to 60 min, as indicated, and substrate cleavage activity was analyzed by agarose gel electrophoresis and real-time RT-PCR as described in Methods. After electrophoresis (right panel), the gel was stained with ethidium bromide, and the bands were quantified by densitometry. Relative band intensity was then graphed against time (left panel). Target (◆), remaining substrate; product 1 (■) and 2 (▲), relative amounts of each of the two cleavage products. Separately, the substrate was quantified by real-time RT-PCR, and the relative amount of remaining substrate (●) was graphed against time. |
doi_str_mv | 10.6084/m9.figshare.21783 |
format | Image |
fullrecord | <record><control><sourceid>datacite_PQ8</sourceid><recordid>TN_cdi_datacite_primary_10_6084_m9_figshare_21783</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_6084_m9_figshare_21783</sourcerecordid><originalsourceid>FETCH-datacite_primary_10_6084_m9_figshare_217833</originalsourceid><addsrcrecordid>eNpjYJA0NNAzM7Aw0c-11EvLTC_OSCxK1TMyNLcw5mSwdc7PLUgsyizOz1PIT1PITS3JyE8pVkjLL1IoLE3MK8lMy0xOLMmEyBZlJuVXVeamKiTnpCaWJaan8jCwpiXmFKfyQmluBkM31xBnD92UxJLE5MyS1PiCoszcxKLKeEODeJAT4nMt42FOiAc7wZgcPQD6m0Q1</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>image</recordtype></control><display><type>image</type><title>Comparison of methods for quantification of ribozyme cleavage</title><source>DataCite</source><creator>Shao, Yu ; Wu, Susan ; Chan, Chi Yu ; Klapper, Jessie R ; Schneider, Erasmus ; Ding, Ye</creator><creatorcontrib>Shao, Yu ; Wu, Susan ; Chan, Chi Yu ; Klapper, Jessie R ; Schneider, Erasmus ; Ding, Ye</creatorcontrib><description>Copyright information:Taken from "A structural analysis of catalytic activities of hammerhead ribozymes"http://www.biomedcentral.com/1471-2105/8/469BMC Bioinformatics 2007;8():469-469.Published online 30 Nov 2007PMCID:PMC2238771. Ribozyme GUC7 was incubated for various lengths of time from 0 to 60 min, as indicated, and substrate cleavage activity was analyzed by agarose gel electrophoresis and real-time RT-PCR as described in Methods. After electrophoresis (right panel), the gel was stained with ethidium bromide, and the bands were quantified by densitometry. Relative band intensity was then graphed against time (left panel). Target (◆), remaining substrate; product 1 (■) and 2 (▲), relative amounts of each of the two cleavage products. Separately, the substrate was quantified by real-time RT-PCR, and the relative amount of remaining substrate (●) was graphed against time.</description><identifier>DOI: 10.6084/m9.figshare.21783</identifier><language>eng</language><publisher>figshare</publisher><subject>Uncategorised</subject><creationdate>2011</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,1894</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.21783$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Shao, Yu</creatorcontrib><creatorcontrib>Wu, Susan</creatorcontrib><creatorcontrib>Chan, Chi Yu</creatorcontrib><creatorcontrib>Klapper, Jessie R</creatorcontrib><creatorcontrib>Schneider, Erasmus</creatorcontrib><creatorcontrib>Ding, Ye</creatorcontrib><title>Comparison of methods for quantification of ribozyme cleavage</title><description>Copyright information:Taken from "A structural analysis of catalytic activities of hammerhead ribozymes"http://www.biomedcentral.com/1471-2105/8/469BMC Bioinformatics 2007;8():469-469.Published online 30 Nov 2007PMCID:PMC2238771. Ribozyme GUC7 was incubated for various lengths of time from 0 to 60 min, as indicated, and substrate cleavage activity was analyzed by agarose gel electrophoresis and real-time RT-PCR as described in Methods. After electrophoresis (right panel), the gel was stained with ethidium bromide, and the bands were quantified by densitometry. Relative band intensity was then graphed against time (left panel). Target (◆), remaining substrate; product 1 (■) and 2 (▲), relative amounts of each of the two cleavage products. Separately, the substrate was quantified by real-time RT-PCR, and the relative amount of remaining substrate (●) was graphed against time.</description><subject>Uncategorised</subject><fulltext>true</fulltext><rsrctype>image</rsrctype><creationdate>2011</creationdate><recordtype>image</recordtype><sourceid>PQ8</sourceid><recordid>eNpjYJA0NNAzM7Aw0c-11EvLTC_OSCxK1TMyNLcw5mSwdc7PLUgsyizOz1PIT1PITS3JyE8pVkjLL1IoLE3MK8lMy0xOLMmEyBZlJuVXVeamKiTnpCaWJaan8jCwpiXmFKfyQmluBkM31xBnD92UxJLE5MyS1PiCoszcxKLKeEODeJAT4nMt42FOiAc7wZgcPQD6m0Q1</recordid><startdate>20111230</startdate><enddate>20111230</enddate><creator>Shao, Yu</creator><creator>Wu, Susan</creator><creator>Chan, Chi Yu</creator><creator>Klapper, Jessie R</creator><creator>Schneider, Erasmus</creator><creator>Ding, Ye</creator><general>figshare</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20111230</creationdate><title>Comparison of methods for quantification of ribozyme cleavage</title><author>Shao, Yu ; Wu, Susan ; Chan, Chi Yu ; Klapper, Jessie R ; Schneider, Erasmus ; Ding, Ye</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_6084_m9_figshare_217833</frbrgroupid><rsrctype>images</rsrctype><prefilter>images</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Uncategorised</topic><toplevel>online_resources</toplevel><creatorcontrib>Shao, Yu</creatorcontrib><creatorcontrib>Wu, Susan</creatorcontrib><creatorcontrib>Chan, Chi Yu</creatorcontrib><creatorcontrib>Klapper, Jessie R</creatorcontrib><creatorcontrib>Schneider, Erasmus</creatorcontrib><creatorcontrib>Ding, Ye</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Shao, Yu</au><au>Wu, Susan</au><au>Chan, Chi Yu</au><au>Klapper, Jessie R</au><au>Schneider, Erasmus</au><au>Ding, Ye</au><format>book</format><genre>unknown</genre><ristype>GEN</ristype><title>Comparison of methods for quantification of ribozyme cleavage</title><date>2011-12-30</date><risdate>2011</risdate><abstract>Copyright information:Taken from "A structural analysis of catalytic activities of hammerhead ribozymes"http://www.biomedcentral.com/1471-2105/8/469BMC Bioinformatics 2007;8():469-469.Published online 30 Nov 2007PMCID:PMC2238771. Ribozyme GUC7 was incubated for various lengths of time from 0 to 60 min, as indicated, and substrate cleavage activity was analyzed by agarose gel electrophoresis and real-time RT-PCR as described in Methods. After electrophoresis (right panel), the gel was stained with ethidium bromide, and the bands were quantified by densitometry. Relative band intensity was then graphed against time (left panel). Target (◆), remaining substrate; product 1 (■) and 2 (▲), relative amounts of each of the two cleavage products. Separately, the substrate was quantified by real-time RT-PCR, and the relative amount of remaining substrate (●) was graphed against time.</abstract><pub>figshare</pub><doi>10.6084/m9.figshare.21783</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | DOI: 10.6084/m9.figshare.21783 |
ispartof | |
issn | |
language | eng |
recordid | cdi_datacite_primary_10_6084_m9_figshare_21783 |
source | DataCite |
subjects | Uncategorised |
title | Comparison of methods for quantification of ribozyme cleavage |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T08%3A07%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-datacite_PQ8&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.au=Shao,%20Yu&rft.date=2011-12-30&rft_id=info:doi/10.6084/m9.figshare.21783&rft_dat=%3Cdatacite_PQ8%3E10_6084_m9_figshare_21783%3C/datacite_PQ8%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |