Monomeric Cyanine Nucleic Acid Stains
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Monomeric Cyanine Nucleic Acid Stains
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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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货号染料类型发射激发波长范围
Y3603细胞不可透过性509 nm491 nm
P3581细胞不可透过性435 nm455 nm
T3602TO-PRO-1 Iodide531 nm515 nm
T3605TO-PRO-3 Iodide661 nm642 nm
Y3607细胞不可透过性631 nm612 nm
货号 Y3603
价格(CNY)
4,489.00
飞享价
Ends: 31-Dec-2025
6,086.00
共减 1,597.00 (26%)
1 mL
添加至购物车
染料类型:
细胞不可透过性
发射:
509 nm
激发波长范围:
491 nm
价格(CNY)
4,489.00
飞享价
Ends: 31-Dec-2025
6,086.00
共减 1,597.00 (26%)
1 mL
添加至购物车
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)

仅供科研使用。不可用于诊断程序。
规格
细胞渗透性非细胞通透性
颜色绿色
最大浓度1 mM
检测方法荧光
染料类型细胞不可透过性
发射509 nm
激发波长范围491 nm
适用于(应用)荧光标记
适用于(设备)荧光显微镜
产品规格管装
产品线YO-PRO
数量1 mL
运输条件室温
标签类型Fluorescent Dye
产品类型核酸染色剂
亚细胞定位细胞核,核酸, Nucleus
Unit Size1 mL
内容与储存
在冷柜(-5°C 至 -30°C)中避光储存。

常见问题解答 (FAQ)

什么是细胞连续凋亡的相对期间时限,我该用什么样的产品去检测不同的凋亡事件?

见本文(https://www.thermofisher.com/content/dam/LifeTech/migration/en/filelibrary/support/bioprobes/bioprobes-65.par.61751.file.dat/bioprobes-65-cellevent.pdf)的表1,在0-4小时的期间,用10 µM喜树碱诱导Jurkat细胞。值得注意的是,这些结果是通过使用单细胞类型和诱导体系研究得到的;对于其他实验体系结果可能不同。凋亡细胞的细胞膜通透性增加,使用YO-PRO-1染料结合碘化丙啶或SYTOX死细胞指示剂能将其与死细胞区分开。其他中期凋亡事件是细胞ROS产物增多(用CellROX reagents,H2DCFDA试剂检测),细胞的pH变化(BCECF, SNARF-1)和钙离子释放(Fluo-4, Fura-2, Indo-1)。任何条件下,没有单个参数能够定义凋亡,因此研究凋亡时最好采用多种参数的方法

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.

What is the relative time-frame of apoptosis progression, and what products can I use to detect the different apoptotic events?

See Table 1 in this article (http://www.thermofisher.com/content/dam/LifeTech/migration/en/filelibrary/support/bioprobes/bioprobes-65.par.61751.file.dat/bioprobes-65-cellevent.pdf) where a Jurkat model system was induced with 10 µM camptothecin for time periods of 0 to 4 hours. It is important to note that these results were studied using a single cell type and induction system; results may differ for other experimental systems. Increased membrane permeability in apoptotic cells can be discriminated from dead cells using YO-PRO-1 dye in combination with propidium iodide or the SYTOX dead cell indicators. Other mid-apoptotic events are increased ROS production (detected with CellROX reagents, H2DCFDA), changes in cellular pH (BCECF, SNARF-1) and calcium release (Fluo-4, Fura-2, Indo-1). No single parameter defines apoptosis under any condition, so it is best to employ a multi-parametric approach when studying apoptosis.

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

引用和文献 (207)

引用和文献
Abstract
Hybridization-induced dequenching of fluorescein-labeled oligonucleotides: a novel strategy for PCR detection and genotyping.
Authors:Vaughn CP,Elenitoba-Johnson KS
Journal:The American journal of pathology
PubMed ID:12819008
Fluorescence-based detection methods are being increasingly utilized in molecular analyses. Sequence-specific fluorescently-labeled probes are favored because they provide specific product identification. The most established fluorescence-based detection systems employ a resonance energy transfer mechanism effected through the interaction of two or more fluorophores or functional groups conjugated to oligonucleotide probes. The ... More
Cloning and functional characterisation of the mouse P2X7 receptor.
Authors:Chessell IP, Simon J, Hibell AD, Michel AD, Barnard EA, Humphrey PP
Journal:FEBS Lett
PubMed ID:9849870
We have isolated a 1785-bp complementary DNA (cDNA) encoding the murine P2X7 receptor subunit from NTW8 mouse microglial cells. The encoded protein has 80%, and 85% homology to the human and rat P2X7 subunits, respectively. Functional properties of the heterologously expressed murine P2X7 homomeric receptor broadly resembled those of the ... 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
Prevalence of bacteria of division TM7 in human subgingival plaque and their association with disease.
Authors:Brinig MM, Lepp PW, Ouverney CC, Armitage GC, Relman DA
Journal:Appl Environ Microbiol
PubMed ID:12620860
Members of the uncultivated bacterial division TM7 have been detected in the human mouth, but little information is available regarding their prevalence and diversity at this site. Human subgingival plaque samples from healthy sites and sites exhibiting various stages of periodontal disease were analyzed for the presence of TM7 bacteria. ... More
Cutting edge: a natural P451L mutation in the cytoplasmic domain impairs the function of the mouse P2X7 receptor.
Authors:Adriouch S, Dox C, Welge V, Seman M, Koch-Nolte F, Haag F
Journal:J Immunol
PubMed ID:12370338
The P2X7 receptor (P2X(7)R) is an ATP-gated channel that mediates apoptosis of cells of the immune system. The capacity of P2X(7)R to form large pores depends on its large cytoplasmic tail, which harbors a putative TNFR-related death domain. Previous transfection studies indicated that mouse P2X(7)R forms pores much less efficiently ... More