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{{Orphan|date=February 2009}}
{{Orphan|date=February 2009}}
'''RiboGreen''' is a proprietary [[fluorescent]] dye that is used in the detection and quantification of [[nucleic acid]]s, including both [[RNA]] and [[DNA]]. It is synthesized and marketed by [[Molecular Probes/Invitrogen]] (a division of [[Life Technologies (Thermo Fisher Scientific)|Life Technologies]]) of [[Eugene, Oregon|Eugene]], [[Oregon]], [[United States]]. In its free form, RiboGreen exhibits little fluorescence and possesses a negligible absorbance signature. When bound to nucleic acids, the dye fluoresces with an intensity that, according to the manufacturer, is several orders of magnitude greater than the unbound form. The fluorescence can be detected by a sensor and the nucleic acid can be quantified. The presence of protein contaminants in the sample of nucleic acids to be tested does not make significant contributions to the absorbance, and thus allows for the addition of [[deoxyribonuclease]]s to the protocol in order to degrade DNA, in the instances where one is only interested in detecting or quantifying RNA.
'''RiboGreen''' is a proprietary [[fluorescent]] dye that is used in the detection and quantification of [[nucleic acid]]s, including both [[RNA]] and [[DNA]]. It is synthesized and marketed by [[Molecular Probes/Invitrogen]] (a division of [[Life Technologies (Thermo Fisher Scientific)|Life Technologies]], now part of [[Thermo Fisher Scientific]]) of [[Eugene, Oregon|Eugene]], [[Oregon]], [[United States]]. In its free form, RiboGreen exhibits little fluorescence and possesses a negligible absorbance signature. When bound to nucleic acids, the dye fluoresces with an intensity that, according to the manufacturer, is several orders of magnitude greater than the unbound form. The fluorescence can be detected by a sensor and the nucleic acid can be quantified. The presence of protein contaminants in the sample of nucleic acids to be tested does not make significant contributions to the absorbance, and thus allows for the addition of [[deoxyribonuclease]]s to the protocol in order to degrade DNA, in the instances where one is only interested in detecting or quantifying RNA.


==References==
==References==
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prostaglandin D2 synthases
prostaglandin D2 synthases
Ian R. JOWSEY*1, Anne M. THOMSON*, Jack U. FLANAGAN*, Paul
Ian R. JOWSEY*1, Anne M. THOMSON*, Jack U. FLANAGAN*, Paul

== External links ==
*[https://www.thermofisher.com/order/catalog/product/R11491 Quant-iT™ RiboGreen® RNA Reagent]
*[https://tools.thermofisher.com/content/sfs/manuals/mp11490.pdf Thermo Fisher Scientific RiboGreen Manual]


[[Category:Staining dyes]]
[[Category:Staining dyes]]

Revision as of 13:21, 5 April 2016

RiboGreen is a proprietary fluorescent dye that is used in the detection and quantification of nucleic acids, including both RNA and DNA. It is synthesized and marketed by Molecular Probes/Invitrogen (a division of Life Technologies, now part of Thermo Fisher Scientific) of Eugene, Oregon, United States. In its free form, RiboGreen exhibits little fluorescence and possesses a negligible absorbance signature. When bound to nucleic acids, the dye fluoresces with an intensity that, according to the manufacturer, is several orders of magnitude greater than the unbound form. The fluorescence can be detected by a sensor and the nucleic acid can be quantified. The presence of protein contaminants in the sample of nucleic acids to be tested does not make significant contributions to the absorbance, and thus allows for the addition of deoxyribonucleases to the protocol in order to degrade DNA, in the instances where one is only interested in detecting or quantifying RNA.

References

J Immunol 2001;167;2869–2878 John I. Gallin Douglas B. Kuhns, Edward L. Nelson, W. Gregory Alvord and Leukotriene B4 Formyl-Methionyl-Leucyl-Phenylalanine or Neutrophils Stimulated with Fibrinogen Induces IL-8 Synthesis in Human

Biochem. J. (2001) 359, 507±516 (Printed in Great Britain) 507 Mammalian class Sigma glutathione S-transferases : catalytic properties and tissue-specific expression of human and rat GSH-dependent prostaglandin D2 synthases Ian R. JOWSEY*1, Anne M. THOMSON*, Jack U. FLANAGAN*, Paul