Monomeric Cyanine Nucleic Acid Stains
Monomeric Cyanine Nucleic Acid Stains
Invitrogen™

Monomeric Cyanine Nucleic Acid Stains

Monomeric Cyanine Nucleic Acid stains are five spectrally distinct dyes for ultrasensitive fluorescence detection of nucleic acid in imaging and flow cytometry. They have bright fluorescence signals, low background, and strong binding affinity with nucleic acid.
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Catalog NumberDye TypeEmissionExcitation Wavelength Range
Y3607YO-PRO-3 Iodide631 nm612 nm
P3581PO-PRO-1 Iodide435 nm455 nm
T3602TO-PRO-1 Iodide531 nm515 nm
T3605TO-PRO-3 Iodide661 nm642 nm
Y3603YO-PRO-1 Iodide509 nm491 nm
Catalog number Y3607
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Dye Type:
YO-PRO-3 Iodide
Emission:
631 nm
Excitation Wavelength Range:
612 nm
Price (CNY)
4,296.00
Online Exclusive
Ends: 31-Dec-2025
5,823.00
Save 1,527.00 (26%)
1 mL
Add to cart
Monomeric Cyanine Nucleic Acid stains allow ultrasensitive fluorescence detection of double-stranded nucleic acids. These high-affinity dyes have low background and bright fluorescence when bound to nucleic acid. They are ideally suited for nuclear staining in flow cytometry and fluorescence microscopy applications in fixed cells, along with nucleic acid detection on solid supports and in electrophoresis applications.

These five spectrally distinct monomeric cyanine nucleic acid stains are high sensitivity fluorescent probes for nucleic acid staining. The carbocyanine monomers have very strong binding affinity for dsDNA, with dissociation constants in the micromolar range. These dyes each comprise a single cyanine dye and a cationic side chain. The carbocyanine monomers are spectrally analogous to the corresponding dimeric cyanine dyes; however, with only two positive charges and one intercalating unit, these dyes exhibit somewhat reduced affinity for nucleic acids relative to the cyanine dimers.

Features of the monomeric cyanine nucleic acid stains:
High affinity—strong binding affinity for dsDNA with dissociation constants in the micromolar range
Low background—negligible fluorescence when not bound to nucleic acids
Large fluorescence enhancement—20- to 1800-fold fluorescence enhancements upon binding to DNA
Bright fluorescence—high extinction coefficients and fluorescence quantum yields resulting in very bright fluorescence signals

Like their dimeric counterparts, these monomeric cyanine dyes are typically impermeant to viable cells and can be used as dead cell indictors, although YO-PRO-1 (Cat. No. Y3603) can be permeant to apoptotic cells, providing a convenient indicator of apoptosis. The monomeric cyanine stains have wide applicability due to their low background and bright fluorescence. Uses include staining of nucleic acids on solid supports, prestaining of samples for gel or capillary electrophoresis, viability detection, and counterstaining in multiple-label experiments.

The fluorescence spectra of the five monomeric cyanine nucleic acid stains cover the entire visible wavelength range and each dye differs in extinction coefficient and quantum yield. These dyes may also be used with ultraviolet trans- or epi-illuminator excitation sources. TO-PRO-1, PO-PRO-1, and YO-PRO-1 dyes exhibit secondary ultraviolet excitation peaks near 275 nm. The monomeric cyanine nucleic acid stains exhibit large degrees of fluorescence enhancement upon binding to DNA (or RNA), varying from 400- to 1800-fold for the “1-series” and 20- to 200-fold for the “3-series.” Consequently, the fluorescence of unbound dye is negligible under most experimental detection conditions.

The monomeric cyanine nucleic acid stains are supplied in a unit size of 1 mL as 1 mM solutions in dimethylsulfoxide (DMSO).

PO-PRO™-1 Iodide (435/455)
The blue-fluorescent PO-PRO-1 stain has excitation/emission maxima ∼435/455 nm when bound to nucleic acid. It can be excited by ultraviolet (UV) excitation sources and the He-Cd 442 nm laser.

YO-PRO™-1 Iodide (491/509)
The green-fluorescent YO-PRO-1 stain has excitation/emission maxima ∼491/509 nm when bound to nucleic acid. It can be excited by ultraviolet (UV) excitation sources and the Ar 488 nm laser. YO-PRO-1 stain has been used to identify apoptotic cells. Apoptotic cells become permeant to YO-PRO-1, but remain impermeant to propidium iodide (Cat. No. P3566) and other dead cell stains. Live cells are not stained with YO-PRO-1, allowing them to be used in subsequent experiments. The YO-PRO-1 nucleic acid stain is also included as an apoptosis indicator in the Vybrant Apoptosis Assay Kit #4 (Cat. No. V13243) and Chromatin Condensation/Membrane Permeability/Dead Cell Apoptosis Kit (Cat. No. V23201).

TO-PRO™-1 Iodide (515/531)
The green-fluorescent TO-PRO-1 stain has excitation/emission maxima ∼515/531 nm when bound to nucleic acid. It can be excited by ultraviolet (UV) excitation sources and the Ar 514 nm laser.

YO-PRO™-3 Iodide (612/631)
The orange-fluorescent YO-PRO-3 stain has excitation/emission maxima ∼612/631 nm when bound to nucleic acid. It can be excited by the He-Ne 594 nm laser.

TO-PRO™-3 Iodide (642/661)
The far-red-fluorescent TO-PRO-3 stain has excitation/emission maxima ∼642/661 nm with fluorescence similar to Alexa Fluor 647 or Cy5 dyes. The long-wavelength fluorescence of TO-PRO-3 stain is well separated from that of commonly used fluorophores, such as the Alexa Fluor dyes, Oregon Green, fluorescein (FITC), rhodamine (TRITC), Texas Red, coumarin (AMCA), Marina Blue, and Pacific Blue dyes. Additionally, long-wavelength light–absorbing dyes such as TO-PRO-3 stain have the advantage that their fluorescence is usually not obscured by the autofluorescence of tissues.

TO-PRO-3 stain is useful as a nuclear counterstain and dead cell indicator in fluorescence microscopy and flow cytometry, and is among the highest-sensitivity probes for nucleic acid detection. TO-PRO-3 gives strong and selective staining of the nucleus in cultured cells and in paraffin sections. Simultaneous labeling with a green-fluorescent SYTO dye and cell-impermeant TO-PRO-3 stain is frequently used to assess cell viability. TO-PRO-3 has a much higher extinction coefficient than DNA-bound propidium iodide and has been used for unique applications such as detecting microbial cells and microorganisms in soil environments.

TO-PRO-3 is also available as room-temperature-stable, ready-to-use solutions:
• NucRed™ Dead 647 ReadyProbes™ Reagent (Cat. No. R37113)
• TO-PRO™ 3 Ready Flow™ Reagent (Cat. No. R37170)

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Cell PermeabilityCell-impermeant
ColorOrange
Concentration1 mM
Detection MethodFluorescence
Dye TypeYO-PRO-3 Iodide
Emission631 nm
Excitation Wavelength Range612 nm
For Use With (Application)Fluorescent Labeling
For Use With (Equipment)Fluorescence Microscope
FormatTube
Product LineYO-PRO
Quantity1 mL
Shipping ConditionRoom Temperature
Storage BufferDMSO
Label TypeFluorescent Dye
Product TypeDead Cell Indicator
SubCellular LocalizationNucleic Acids, Nucleus
Unit Size1 mL
Contents & Storage
Store in freezer at -5°C to -30°C and protect from light.

Frequently asked questions (FAQs)

What is the suggested working concentration for Monomeric Cyanine Nucleic Acid Stains (Cat. Nos. T3605, P3581, T3602, Y3603, Y3607) for fluorescence microscopy?

For fluorescence microscopy, the working concentration of Monomeric Cyanine Nucleic Acid Stains (Cat. Nos. T3605, P3581, T3602, Y3603, Y3607) is typically 1 - 10 µM. You may need to titrate the dye solution to optimize the working concentration for your sample type and application.

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

What is the suggested working concentration for Monomeric Cyanine Nucleic Acid Stains (Cat. Nos. T3605, P3581, T3602, Y3603, Y3607) for flow cytometry?

For flow cytometry, the working concentration of Monomeric Cyanine Nucleic Acid Stains (Cat. Nos. T3605, P3581, T3602, Y3603, Y3607) is typically 25 nM - 1 µM. You may need to titrate the dye solution to optimize the working concentration for your sample type and application.

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

Citations & References (9)

Citations & References
Abstract
Active caspase-8 translocates into the nucleus of apoptotic cells to inactivate poly(ADP-ribose) polymerase-2.
Authors:Benchoua A, Couriaud C, Guégan C, Tartier L, Couvert P, Friocourt G, Chelly J, Ménissier-de Murcia J, Onténiente B
Journal:J Biol Chem
PubMed ID:12065591
'Caspase-8 is the prototypic initiator of the death domain receptor pathway of apoptosis. Here, we report that caspase-8 not only triggers and amplifies the apoptotic process at cytoplasmic sites but can also act as an executioner at nuclear levels. In a murine model of acute ischemia, caspase-8 is relocated into ... More
P2X purinergic receptor channel expression and function in bovine aortic endothelium.
Authors:Ramirez AN, Kunze DL
Journal:Am J Physiol Heart Circ Physiol
PubMed ID:12003818
'We examined bovine aortic endothelial cells (BAECs) for the functional expression of P2X receptors, the ATP-gated cation channels. We identified the P2X subtypes present in BAECs using RT-PCR. mRNA was present for only three of seven family members: P2X4, P2X5, and P2X7. We then characterized agonist-activated currents in whole cell ... More
Versatile low-viscosity sieving matrices for nondenaturing DNA separations using capillary array electrophoresis.
Authors:Madabhushi RS, Vainer M, Dolnik V, Enad S, Barker DL, Harris DW, Mansfield ES
Journal:Electrophoresis
PubMed ID:9059830
'The high-resolution separation of double-stranded DNA (dsDNA) has important applications in physical mapping strategies and in the analysis of polymerase chain reaction (PCR) products. Although high-resolution separations of dsDNA by capillary electrophoresis (CE) have been reported, pulsed fields were required to achieve complete resolution of DNA fragments beyond 23 kilobase ... More
TO-PRO-3 is an optimal fluorescent dye for nuclear counterstaining in dual-colour FISH on paraffin sections.
Authors:Bink K, Walch A, Feuchtinger A, Eisenmann H, Hutzler P, Höfler H, Werner M
Journal:Histochem Cell Biol
PubMed ID:11405057
Confocal laser scanning microscopy (CLSM) is an extensive but reliable tool for assessing the hybridisation signals in fluorescence in situ hybridisation (FISH). Most CLSMs are equipped with an argon-laser and a helium/neon-laser illumination system with excitation wavelengths of 488, 543 and 633 nm. A protocol for an optimal nuclear counterstaining ... More
Fluorescence enhancement of DNA-bound TO-PRO-3 by incorporation of bromodeoxyuridine to monitor cell cycle kinetics.
Authors:Beisker W, Weller-Mewe EM, Nüsse M
Journal:Cytometry
PubMed ID:10520203
BACKGROUND:The detection of DNA-incorporated bromodeoxyuridine (BrdUrd) in mammalian cells is a well-known and important technique to study cell cycle. The use of TO-PRO-3 for detection of BrdUrd substitution of DNA by dual-laser flow cytometry has been investigated. METHODS:Fluorescence enhancement of TO-PRO-3 in BrdUrd-labeled cells is registered in combination with the ... More