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
Hauptverfasser: Jones, Laurie J., Yue, Stephen T., Cheung, Ching-Ying, Singer, Victoria L.
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container_end_page 374
container_issue 2
container_start_page 368
container_title Analytical biochemistry
container_volume 265
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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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 &gt;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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