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Rhodamine Red&trade; C<sub>2</sub> Maleimide
Citations & References (4)
Invitrogen™

Rhodamine Red™ C2 Maleimide

Rhodamine Red™ C2 maleimide
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Catalog NumberQuantity
R6029
also known as R-6029
5 mg
Catalog number R6029
also known as R-6029
Price (INR)
-
Quantity:
5 mg

The thiol-reactive Rhodamine Red™ C2 maleimide can be used to create red-fluorescent bioconjugates with excitation/emission maxima ∼560/580 nm.

For Research Use Only. Not for use in diagnostic procedures.

Specifications
Chemical ReactivityThiol
Emission580
Excitation560
Label or DyeRhodamine Red™, Rhodamine Red™ C2 maleimide
Product TypeMaleimide
Quantity5 mg
Reactive MoietyMaleimide
Shipping ConditionRoom Temperature
Label TypeClassic Dyes
Product LineRhodamine Red
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.

Frequently asked questions (FAQs)

What is the excitation and emission wavelength for rhodamine?

Rhodamine is a generic term for a wide variety of cationic dyes whose fluorescence emission can range from green, orange to red. The table below lists the excitation and emission maxima (nm), as well as molar extinction coefficients (“EC”; cm-1 M-1), for various rhodamine dyes (data derived with dye dissolved in methanol).

Dye Excitation Emission EC
Rhodamine B 568 583 88,000
Rhodamine 123 507 529 101,000
Rhodamine 110 499 521 92,000
Rhodamine 6G 528 551 105,000
XRITC 572 596 92,000


Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Citations & References (4)

Citations & References
Abstract
A biosensor for inorganic phosphate using a rhodamine-labeled phosphate binding protein.
Authors:Okoh MP, Hunter JL, Corrie JE, Webb MR
Journal:Biochemistry
PubMed ID:17144669
'A novel biosensor for inorganic phosphate (Pi) has been developed based on the phosphate binding protein of Escherichia coli. Two cysteine mutations were introduced and labeled with 6-iodoacetamidotetramethylrhodamine. When physically close to each other and correctly oriented, two rhodamine dyes interact to form a noncovalent dimer. In this state, they ... More
Dependence of fluorescence intensity on the spectral overlap between fluorophores and plasmon resonant single silver nanoparticles.
Authors:Chen Y, Munechika K, Ginger DS
Journal:Nano Lett
PubMed ID:17315937
'We investigate the fluorescence from dyes coupled to individual DNA-functionalized metal nanoparticles. We use single-particle darkfield scattering and fluorescence microscopy to correlate the fluorescence intensity of the dyes with the localized surface plasmon resonance (LSPR) spectra of the individual metal nanoparticles to which they are attached. For each of three ... More
Filling the green gap of the major light-harvesting chlorophyll a/b complex by covalent attachment of Rhodamine Red.
Authors:Gundlach K, Werwie M, Wiegand S, Paulsen H,
Journal:Biochim Biophys Acta
PubMed ID:19619502
'The major light-harvesting chlorophyll a/b complex (LHCII) greatly enhances the efficiency of photosynthesis in green plants. Recombinant LHCII can be assembled in vitro from its denatured, bacterially expressed apoprotein and plant pigments. This makes it an interesting candidate for biomimetic light-harvesting in photovoltaic applications. Due to its almost 20 pigments ... More
Thiol-reactive dyes for fluorescence labeling of proteomic samples.
Authors:Tyagarajan K, Pretzer E, Wiktorowicz JE
Journal:Electrophoresis
PubMed ID:12874870
Covalent derivatization of proteins with fluorescent dyes prior to separation is increasingly used in proteomic research. This paper examines the properties of several commercially available iodoacetamide and maleimide dyes and discusses the conditions and caveats for their use in labeling of proteomic samples. The iodoacetamide dyes BODIPY TMR cadaverine IA ... More