Dimeric Cyanine Nucleic Acid Stains
Dimeric Cyanine Nucleic Acid Stains
Invitrogen™

Dimeric Cyanine Nucleic Acid Stains

Dimeric Cyanine Nucleic Acid stains are eight spectrally distinct dyes for ultrasensitive fluorescence detection of nucleic acid in imaging and flow cytometry. They are cell-impermeant and have bright fluorescence signals, low background, and strong binding affinity with nucleic acid.
製品番号(カタログ番号)染色剤タイプ発光励起波長域
N7565細胞非透過性456, 481, 509, 533, 570, 602, 631, 660 nm436, 442, 488, 514, 543, 568, 594, 633 nm
B3582細胞非透過性481 nm462⁄481
B3586細胞非透過性602 nm570⁄602
P3580細胞非透過性456 nm434 nm
P3584細胞非透過性570 nm534⁄570
T3600TOTO-1 Iodide533 nm514 nm
T3604TOTO-3 Iodide660 nm642 nm
Y3601細胞非透過性509 nm491⁄509
Y3606細胞非透過性631 nm612⁄631
製品番号(カタログ番号) N7565
価格(JPY)
56,100
線上優惠
Ends: 27-Mar-2026
93,500
割引額 37,400 (40%)
Each
お問い合わせください ›
染色剤タイプ:
細胞非透過性
発光:
456, 481, 509, 533, 570, 602, 631, 660 nm
励起波長域:
436, 442, 488, 514, 543, 568, 594, 633 nm
Dimeric Cyanine Nucleic Acid stains are cell-impermeant dyes that enable ultrasensitive fluorescence detection of nucleic acid. These dyes have very bright fluorescence signals, strong binding affinity for dsDNA, and large fluorescence enhancement upon binding to nucleic acid. They can be used as dead cell indicators and nuclear counterstains in fluorescence microscopy and flow cytometry. Dimeric cyanine nucleic acid dyes can also be used to stain nucleic acids on solid supports, as well as in capillary and gel electrophoresis applications.

These eight spectrally distinct dimeric cyanine nucleic acid stains are among the highest sensitivity fluorescent probes available for nucleic acid staining. The carbocyanine dimers have very strong binding affinity for dsDNA, with dissociation constants in the micromolar range and nucleic acid-binding affinities greater than their parent monomer dyes. In addition to their high affinity for nucleic acids, cyanine dimers are essentially nonfluorescent in the absence of nucleic acids and exhibit 100- to 1000-fold fluorescence enhancements upon binding to DNA. The extinction coefficients and fluorescence quantum yields of the cyanine dimers bound to DNA are high, resulting in very bright fluorescence signals.

Features of the dimeric cyanine nucleic acid stains:
High affinity—strong binding affinity for dsDNA with dissociation constants in the micromolar range
Low background—nonfluorescent in the absence of nucleic acids
Large fluorescence enhancement—100- to 1000-fold fluorescence enhancements upon binding to DNA
Bright fluorescence—high extinction coefficients and fluorescence quantum yields resulting in very bright fluorescence signals

The dimeric cyanine dyes are useful for many applications including fluorescence microscopy and flow cytometry. These dyes are impermeant to viable cells and can be used as dead cell indictors. Their bright fluorescence signals and low backgrounds make them ideal for staining nucleic acids on solid supports, such as microarrays. They are also useful as nuclear and chromosome counterstains for multicolor fluorescence labeling experiments such as in immunohistochemistry (IHC) and immunocytochemistry (ICC). Prestaining nucleic acid samples prior to gel or capillary electrophoresis is also possible due to the extraordinary stability of the dye-nucleic acid complexes.

The dimeric cyanine nucleic acid stains are supplied in a unit size of 200 μL as 1 mM solutions in dimethylsulfoxide (DMSO) or dimethylformamide (DMF) for the POPO-3 stain. The fluorescence spectra of the eight dimeric cyanine nucleic acid stains cover the entire visible wavelength range and each dye differs in extinction coefficient and quantum yield.

POPO™-1 Iodide (434/456)
The blue-fluorescent POPO-1 stain has excitation/emission maxima ∼434/456 nm when bound to dsDNA in aqueous solution. It can be excited by ultraviolet (UV) excitation sources and the Hg arc (only) 436 nm laser.

BOBO™-1 Iodide (462/481)
The blue-fluorescent BOBO-1 stain has excitation/emission maxima ∼462/481 nm when bound to dsDNA in aqueous solution. It can be excited by ultraviolet (UV) excitation sources and the He-Cd 442 nm laser.

YOYO™-1 Iodide (491/509)
One of our highest affinity nucleic acid stains, the green-fluorescent YOYO-1 stain shows over 1000-fold increase in fluorescence when bound to dsDNA. It has excitation/emission maxima ∼491/509 nm when bound to nucleic acids and can be excited by ultraviolet (UV) excitation sources and the Ar 488 nm laser. YOYO-1 stain has proved extremely useful in the analysis of single molecules of DNA and is used in super-resolution microscopy applications such as STORM.

TOTO™-1 Iodide (514/533)
The green-fluorescent TOTO-1 stain has excitation/emission maxima ∼514/533 nm when bound to dsDNA in aqueous solution. The DNA-bound TOTO-1 dye also has a short-wavelength peak at ∼275 nm and can be excited by ultraviolet (UV) excitation sources and the Ar 514 nm laser.

POPO™-3 Iodide (534/570)
The yellow-fluorescent POPO-3 stain has excitation/emission maxima ∼534/570 nm when bound to dsDNA in aqueous solution. It can be excited by the He-Ne 543 nm laser.

BOBO™-3 Iodide (570/602)
The orange-fluorescent BOBO-3 stain has excitation/emission maxima ∼570/602 nm when bound to dsDNA in aqueous solution. It can be excited by the Kr 568 nm laser.

YOYO™-3 Iodide (612/631)
The orange-fluorescent YOYO-3 stain has excitation/emission maxima ∼612/631 nm when bound to dsDNA in aqueous solution. It can be excited by the He-Ne 594 nm laser.

TOTO™-3 Iodide (642/660)
The far-red fluorescent TOTO-3 stain has excitation/emission maxima ∼640/660 nm when bound to dsDNA in aqueous solution. It can be excited by the He-Ne 633 nm laser. The long-wavelength fluorescence of TOTO-3 stain is similar to Alexa Fluor 647 or Cy5 dyes and is well separated from that of commonly used fluorophores, such as 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 TOTO-3 stain have the advantage that their fluorescence is usually not obscured by the autofluorescence of tissues.

TOTO-3 stain has high selectivity for nuclear over cytoplasmic staining, making it useful as a nuclear counterstain and dead cell indicator, and is among the highest-sensitivity probes for nucleic acid detection. TOTO-3 stain gives strong and selective nuclear staining in cultured cells and in paraffin sections. Simultaneous labeling with a green-fluorescent SYTO dye and cell-impermeant TOTO-3 stain is frequently used to assess cell viability. TOTO-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.

Nucleic Acid Stains Dimer Sampler Kit
For researchers designing new applications, the Nucleic Acid Stains Dimer Sampler Kit provides samples of the eight spectrally distinct analogs of the dimeric cyanine dyes for testing. This kit contains 25 μL each of the following high-affinity nucleic acid stains based upon symmetric dimers of cyanine dyes:
• BOBO-1 iodide (Cat. No. B3582)
• BOBO-3 iodide (Cat. No. B3586)
• POPO-1 iodide (Cat. No. P3580)
• POPO-3 iodide (Cat. No. P3584)
• TOTO-1 iodide (Cat. No. T3600)
• TOTO-3 iodide (Cat. No. T3604)
• YOYO-1 iodide (Cat. No. Y3601)
• YOYO-3 iodide (Cat. No. Y3603)

研究用途にのみご使用ください。ヒトまたは動物の治療もしくは診断用には使用できません。
仕様
細胞透過性Cell-impermeant
オレンジ, 緑, 黄, 赤, 青
検出法蛍光
染色剤タイプ細胞非透過性
発光456, 481, 509, 533, 570, 602, 631, 660 nm
励起波長域436, 442, 488, 514, 543, 568, 594, 633 nm
使用対象(アプリケーション)Fluorescent Labeling
使用対象 (装置)蛍光顕微鏡
フォーマットKit
製品ラインBOBO, POPO, TOTO, YOYO
数量25 μL kit
出荷条件室温
標識タイプFluorescent Dye
製品タイプStains Dimer Sampler Kit
SubCellular Localization核酸
Unit SizeEach
組成および保存条件
別々のバイアルに各色素のDMSO中の1 mM溶液が25 μL含まれます。
  • フリーザー(-5℃~-30℃)に保存し、遮光してください。
  • 引用および参考文献 (388)

    引用および参考文献
    Abstract
    Design and characterization of a compact dual channel virus counter.
    Authors:Stoffel CL,Kathy RF,Rowlen KL
    Journal:Cytometry. Part A : the journal of the International Society for Analytical Cytology
    PubMed ID:15830378
    Cell-to-cell movement of potato spindle tuber viroid.
    Authors:Ding B, Kwon MO, Hammond R, Owens R
    Journal:Plant J
    PubMed ID:9375403
    Viroids are non-translatable, autonomously replicating circular RNAs that infect only plants. An important component of the viroid infection process is cell-to-cell movement; however, there is virtually no information available about the pathways and mechanisms of this process. In this study, potato spindle tuber viroid (PSTVd) has been used as a ... More
    Quantitation of polymerase chain reaction products by capillary electrophoresis using laser fluorescence.
    Authors:Butler JM, McCord BR, Jung JM, Wilson MR, Budowle B, Allen RO
    Journal:J Chromatogr B Biomed Appl
    PubMed ID:7820255
    In samples where the amount of DNA is limited, the polymerase chain reaction (PCR) can amplify specific regions of the DNA. A quantitative analysis of the PCR product would be desirable to ensure sufficient DNA is available for analysis. In this study, we examine the use of capillary electrophoresis (CE) ... More
    Development and evaluation of an automated workstation for single nucleotide polymorphism discrimination using bacterial magnetic particles.
    Authors:Tanaka T, Maruyama K, Yoda K, Nemoto E, Udagawa Y, Nakayama H, Takeyama H, Matsunaga T
    Journal:Biosens Bioelectron
    PubMed ID:14615090
    We designed an automated workstation for magnetic particle-based single nucleotide polymorphism (SNP) discrimination of ALDH genotypes. Bacterial magnetic particles (BMPs) extracted from Magnetospirillum magneticum AMB-1 were used as DNA carriers. The principle for SNP discrimination in this study was based on fluorescence resonance energy transfer (FRET) between FITC (donor) and ... More
    Cyclin G2 associates with protein phosphatase 2A catalytic and regulatory B' subunits in active complexes and induces nuclear aberrations and a G1/S phase cell cycle arrest.
    Authors:Bennin David A; Don Aruni S Arachchige; Brake Tiffany; McKenzie Jennifer L; Rosenbaum Heidi; Ortiz Linette; DePaoli-Roach Anna A; Horne Mary C;
    Journal:J Biol Chem
    PubMed ID:11956189
    Cyclin G2, together with cyclin G1 and cyclin I, defines a novel cyclin family expressed in terminally differentiated tissues including brain and muscle. Cyclin G2 expression is up-regulated as cells undergo cell cycle arrest or apoptosis in response to inhibitory stimuli independent of p53 (Horne, M., Donaldson, K., Goolsby, G., ... More