RNA Quantitation by Fluorescence-Based Solution Assay: RiboGreen Reagent Characterization
We describe the development of a sensitive fluorescence-based solution assay for RNA using a new dye, RiboGreen RNA quantitation reagent. RiboGreen reagent exhibits >1000-fold fluorescence enhancement and high quantum yield (0.65) upon binding nucleic acids, with excitation and emission maxima ne...
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Veröffentlicht in: | Analytical biochemistry 1998-12, Vol.265 (2), p.368-374 |
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creator | Jones, Laurie J. Yue, Stephen T. Cheung, Ching-Ying Singer, Victoria L. |
description | We describe the development of a sensitive fluorescence-based solution assay for RNA using a new dye, RiboGreen RNA quantitation reagent. RiboGreen reagent exhibits >1000-fold fluorescence enhancement and high quantum yield (0.65) upon binding nucleic acids, with excitation and emission maxima near those of fluorescein. Unbound dye is essentially nonfluorescent and has a large extinction coefficient (67,000 cm−1M−1). The RiboGreen assay allows detection of as little as 1.0 ng/ml RNA in a standard fluorometer, filter fluorometer, or fluorescence microplate reader—surpassing the sensitivity achieved with ethidium bromide by 200-fold. The linear quantitation range for RiboGreen reagent extends over three orders of magnitude in RNA concentration. Using 750 nM RiboGreen reagent, we quantitated 20 ng/ml to 1.0 μg/ml RNA. By diluting the reagent to 75 nM, we could quantitate 1.0 to 50 ng/ml RNA. Both assay ranges exhibited linear fluorescence increases versus RNA concentration (r2= 0.999). Assay linearity was maintained in the presence of salts, protein, urea, ethanol, chloroform, agarose, and some detergents. Several different RNA types yielded similar signal intensities and detection sensitivities. The assay is easy to use, rapid, and readily adaptable for automation. |
doi_str_mv | 10.1006/abio.1998.2914 |
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RiboGreen reagent exhibits >1000-fold fluorescence enhancement and high quantum yield (0.65) upon binding nucleic acids, with excitation and emission maxima near those of fluorescein. Unbound dye is essentially nonfluorescent and has a large extinction coefficient (67,000 cm−1M−1). The RiboGreen assay allows detection of as little as 1.0 ng/ml RNA in a standard fluorometer, filter fluorometer, or fluorescence microplate reader—surpassing the sensitivity achieved with ethidium bromide by 200-fold. The linear quantitation range for RiboGreen reagent extends over three orders of magnitude in RNA concentration. Using 750 nM RiboGreen reagent, we quantitated 20 ng/ml to 1.0 μg/ml RNA. By diluting the reagent to 75 nM, we could quantitate 1.0 to 50 ng/ml RNA. Both assay ranges exhibited linear fluorescence increases versus RNA concentration (r2= 0.999). Assay linearity was maintained in the presence of salts, protein, urea, ethanol, chloroform, agarose, and some detergents. Several different RNA types yielded similar signal intensities and detection sensitivities. The assay is easy to use, rapid, and readily adaptable for automation.</description><identifier>ISSN: 0003-2697</identifier><identifier>EISSN: 1096-0309</identifier><identifier>DOI: 10.1006/abio.1998.2914</identifier><identifier>PMID: 9882416</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>ethidium bromide ; fluorescence ; Fluorescent Dyes - chemistry ; Indicators and Reagents - chemistry ; nucleic acid stain ; RiboGreen ; RNA - analysis ; RNA detection ; RNA quantitation ; Sensitivity and Specificity ; Spectrometry, Fluorescence</subject><ispartof>Analytical biochemistry, 1998-12, Vol.265 (2), p.368-374</ispartof><rights>1998 Academic Press</rights><rights>Copyright 1998 Academic Press.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-55b20680e86d26a288400d58db82117ca6ef9e364c3f63cff4fabf7fc59726903</citedby><cites>FETCH-LOGICAL-c405t-55b20680e86d26a288400d58db82117ca6ef9e364c3f63cff4fabf7fc59726903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/abio.1998.2914$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9882416$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jones, Laurie J.</creatorcontrib><creatorcontrib>Yue, Stephen T.</creatorcontrib><creatorcontrib>Cheung, Ching-Ying</creatorcontrib><creatorcontrib>Singer, Victoria L.</creatorcontrib><title>RNA Quantitation by Fluorescence-Based Solution Assay: RiboGreen Reagent Characterization</title><title>Analytical biochemistry</title><addtitle>Anal Biochem</addtitle><description>We describe the development of a sensitive fluorescence-based solution assay for RNA using a new dye, RiboGreen RNA quantitation reagent. RiboGreen reagent exhibits >1000-fold fluorescence enhancement and high quantum yield (0.65) upon binding nucleic acids, with excitation and emission maxima near those of fluorescein. Unbound dye is essentially nonfluorescent and has a large extinction coefficient (67,000 cm−1M−1). The RiboGreen assay allows detection of as little as 1.0 ng/ml RNA in a standard fluorometer, filter fluorometer, or fluorescence microplate reader—surpassing the sensitivity achieved with ethidium bromide by 200-fold. The linear quantitation range for RiboGreen reagent extends over three orders of magnitude in RNA concentration. Using 750 nM RiboGreen reagent, we quantitated 20 ng/ml to 1.0 μg/ml RNA. By diluting the reagent to 75 nM, we could quantitate 1.0 to 50 ng/ml RNA. Both assay ranges exhibited linear fluorescence increases versus RNA concentration (r2= 0.999). Assay linearity was maintained in the presence of salts, protein, urea, ethanol, chloroform, agarose, and some detergents. Several different RNA types yielded similar signal intensities and detection sensitivities. The assay is easy to use, rapid, and readily adaptable for automation.</description><subject>ethidium bromide</subject><subject>fluorescence</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Indicators and Reagents - chemistry</subject><subject>nucleic acid stain</subject><subject>RiboGreen</subject><subject>RNA - analysis</subject><subject>RNA detection</subject><subject>RNA quantitation</subject><subject>Sensitivity and Specificity</subject><subject>Spectrometry, Fluorescence</subject><issn>0003-2697</issn><issn>1096-0309</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kD1PwzAQhi0EgvKxsiFlYks5J45rs5WKAhICUWBgshznDEZpDHaCVH49Ca3YmG5433t09xByTGFMAfiZLp0fUynFOJOUbZERBclTyEFukxEA5GnG5WSP7Mf4DkApK_gu2ZVCZIzyEXlZ3E2Th043rWt163yTlKtkXnc-YDTYGEwvdMQqefR19xtPY9Sr82ThSn8VEJtkgfoVmzaZvemgTYvBff-CDsmO1XXEo808IM_zy6fZdXp7f3Uzm96mhkHRpkVRZsAFoOBVxnUmBAOoClGVIqN0YjRHKzHnzOSW58ZaZnVpJ9YUctJ_BvkBOV1zP4L_7DC2aun60-taN-i7qLikOWNF1hfH66IJPsaAVn0Et9RhpSiowaUaXKrBpRpc9gsnG3JXLrH6q2_k9blY59i_9-UwqGjc4KxyAU2rKu_-Q_8AuNKDQQ</recordid><startdate>19981215</startdate><enddate>19981215</enddate><creator>Jones, Laurie J.</creator><creator>Yue, Stephen T.</creator><creator>Cheung, Ching-Ying</creator><creator>Singer, Victoria L.</creator><general>Elsevier Inc</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>19981215</creationdate><title>RNA Quantitation by Fluorescence-Based Solution Assay: RiboGreen Reagent Characterization</title><author>Jones, Laurie J. ; Yue, Stephen T. ; Cheung, Ching-Ying ; Singer, Victoria L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-55b20680e86d26a288400d58db82117ca6ef9e364c3f63cff4fabf7fc59726903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>ethidium bromide</topic><topic>fluorescence</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Indicators and Reagents - chemistry</topic><topic>nucleic acid stain</topic><topic>RiboGreen</topic><topic>RNA - analysis</topic><topic>RNA detection</topic><topic>RNA quantitation</topic><topic>Sensitivity and Specificity</topic><topic>Spectrometry, Fluorescence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jones, Laurie J.</creatorcontrib><creatorcontrib>Yue, Stephen T.</creatorcontrib><creatorcontrib>Cheung, Ching-Ying</creatorcontrib><creatorcontrib>Singer, Victoria L.</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>Analytical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jones, Laurie J.</au><au>Yue, Stephen T.</au><au>Cheung, Ching-Ying</au><au>Singer, Victoria L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>RNA Quantitation by Fluorescence-Based Solution Assay: RiboGreen Reagent Characterization</atitle><jtitle>Analytical biochemistry</jtitle><addtitle>Anal Biochem</addtitle><date>1998-12-15</date><risdate>1998</risdate><volume>265</volume><issue>2</issue><spage>368</spage><epage>374</epage><pages>368-374</pages><issn>0003-2697</issn><eissn>1096-0309</eissn><abstract>We describe the development of a sensitive fluorescence-based solution assay for RNA using a new dye, RiboGreen RNA quantitation reagent. RiboGreen reagent exhibits >1000-fold fluorescence enhancement and high quantum yield (0.65) upon binding nucleic acids, with excitation and emission maxima near those of fluorescein. Unbound dye is essentially nonfluorescent and has a large extinction coefficient (67,000 cm−1M−1). The RiboGreen assay allows detection of as little as 1.0 ng/ml RNA in a standard fluorometer, filter fluorometer, or fluorescence microplate reader—surpassing the sensitivity achieved with ethidium bromide by 200-fold. The linear quantitation range for RiboGreen reagent extends over three orders of magnitude in RNA concentration. Using 750 nM RiboGreen reagent, we quantitated 20 ng/ml to 1.0 μg/ml RNA. By diluting the reagent to 75 nM, we could quantitate 1.0 to 50 ng/ml RNA. Both assay ranges exhibited linear fluorescence increases versus RNA concentration (r2= 0.999). Assay linearity was maintained in the presence of salts, protein, urea, ethanol, chloroform, agarose, and some detergents. Several different RNA types yielded similar signal intensities and detection sensitivities. The assay is easy to use, rapid, and readily adaptable for automation.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>9882416</pmid><doi>10.1006/abio.1998.2914</doi><tpages>7</tpages></addata></record> |
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subjects | ethidium bromide fluorescence Fluorescent Dyes - chemistry Indicators and Reagents - chemistry nucleic acid stain RiboGreen RNA - analysis RNA detection RNA quantitation Sensitivity and Specificity Spectrometry, Fluorescence |
title | RNA Quantitation by Fluorescence-Based Solution Assay: RiboGreen Reagent Characterization |
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