SYTO™ Green Fluorescent Nucleic Acid Stains
SYTO™ Green Fluorescent Nucleic Acid Stains
Invitrogen™

SYTO™ Green Fluorescent Nucleic Acid Stains

SYTO Green Fluorescent Nucleic Acid Stains exhibit bright, green fluorescence upon binding to nucleic acids. These dyes are cell-permeant and can be used to stain RNA and DNA in live cells, dead cells, and bacteria.
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카탈로그 번호염료 유형수량
S7576SYTO 14 Green250 μL
S34854SYTO 9 Green100 μL
S7573SYTO 11 Green250 μL
S7574SYTO 12 Green315 μL
S7575SYTO 13 Green250 μL
S7578SYTO 16 Green250 μL
S7556SYTO 21 Green250 μL
S7559SYTO 24 Green250 μL
S34855SYTO BC Green100 μL
S32703SYTO RNASelect Green100 μL
S7572SYTO Green Dyes 11-14, 16, 21, 24, and 251 Kit (50 μL each)
카탈로그 번호 S7576
제품 가격(KRW)
440,000
Online offer
Ends: 31-Dec-2025
517,000
할인액 77,000 (15%)
Each
카트에 추가하기
염료 유형:
SYTO 14 Green
수량:
250 μL
제품 가격(KRW)
440,000
Online offer
Ends: 31-Dec-2025
517,000
할인액 77,000 (15%)
Each
카트에 추가하기

The SYTO Green Fluorescent Nucleic Acid Stains exhibit bright, green fluorescence upon binding to nucleic acids. These dyes are cell-permeant and can be used to stain RNA and DNA in live cells, dead cells, and bacteria. Because the dye characteristics and staining pattern of the SYTO dyes may vary, we offer 10 different SYTO Green Fluorescent Nucleic Acid Stains available individually along with the SYTO Green Fluorescent Nucleic Acid Stain Sampler Kit #1 (containing SYTO 11–14, 16, 21, 24, and 25) to enable researchers to find the most appropriate green-fluorescent SYTO stain for their system . We also provide the SYTOX Green Nucleic Acid Stain (Cat. No. S7020 and R37109), which is a cell-impermeant green-fluorescent stain used for staining dead cells or performing nuclear counterstaining in fixed cells.

SYTO Green Fluorescent Nucleic Acid Stains are cell-permeant nucleic acid stains that show a large fluorescence enhancement upon binding nucleic acids. The SYTO dyes can be used to stain RNA and DNA in both live and dead eukaryotic cells, as well as in Gram-positive and Gram-negative bacteria.

The SYTO stains share several important characteristics:

  • Permeability to virtually all cell membranes, including mammalian cells and bacteria
  • High molar absorptivity, with extinction coefficients >50,000 cm-1 M-1 at visible absorption maxima
  • Extremely low intrinsic fluorescence, with quantum yields typically <0.01 when not bound to nucleic acids
  • Quantum yields that are typically >0.4 when bound to nucleic acids.

SYTO Green-Fluorescent Nucleic Acid Stains excitation/emission wavelengths

  • SYTO 9—RNA 486/501 nm; DNA 485/498 nm
  • SYTO 11—RNA 510/530 nm; DNA 508/527 nm
  • SYTO 12—RNA 500/519 nm; DNA 499/522 nm
  • SYTO 13—RNA 491/514 nm; DNA 488/509 nm
  • SYTO 14—RNA 521/547 nm; DNA 517/549 nm
  • SYTO 16—RNA 494/525 nm; DNA 488/518 nm
  • SYTO 21—DNA 494/517 nm
  • SYTO 24—DNA 490/515 nm
  • SYTO BC—RNA 487/504 nm; DNA 485/500 nm
  • SYTO RNASelect—RNA 490/530 nm

SYTO dyes differ from each other in one or more characteristics, including cell permeability, fluorescence enhancement upon binding nucleic acids, excitation and emission spectra, DNA/RNA selectivity, and binding affinity. The SYTO dyes are compatible with a variety of fluorescence-based instruments that use laser excitation or a conventional broadband illumination source (e.g., mercury- and xenon-arc lamps). Filter sets that are suitable for imaging cells labeled with fluorescein (FITC), Alexa Fluor 488, or GFP will work well for imaging cells stained with SYTO Green Nucleic Acid Stains.

SYTO nucleic acid stains have been used in diverse applications from staining DNA spotted on microarrays to staining live and fixed cells. The SYTO dyes do not act exclusively as nuclear stains in live cells and should not be equated with DNA-selective compounds such as DAPI (Cat. Nos. D1306, D21490) or Hoechst 33342 (Cat. Nos. H1399, H3570), which stain nuclei in live animal cells. Eukaryotic cells incubated with SYTO dyes generally show cytoplasmic or mitochondrial staining, as well as nuclear staining. The SYTO Green Fluorescent Nucleic Acid Stains have proven valuable in a broad range of research applications as well as used in flow cytometry and fluorescence microscopy.

Specific staining applications for some of the SYTO Green Fluorescent Nucleic Acid Stains

The SYTO 9 stain has been shown to stain live and dead Gram-positive and Gram-negative bacteria. It is a component of the LIVE/DEAD BacLight Bacterial Viability Kits (Cat. Nos. L7007, L7012, L13152).

The SYTO 11 stain (Cat. No. S7573) has been used in conjunction with time-lapse microscopy to examine the cleavage orientation of dividing cells in the developing cerebral cortex.

The SYTO 13 stain (Cat. No. S7575) has been used in combination with propidium iodide (Cat. Nos. P1304, P3566) to monitor glutamate-induced necrosis in cerebellar granule cells.

The SYTO 14 stain (Cat. No. S7576) binds to cytoplasmic RNA, allowing its use in tracking RNA granule transport in living neurons.

Several reports describe the use of SYTO dyes for detecting apoptosis. A series of SYTO nucleic acid stains was screened for the ability to discriminate between apoptotic and non-apoptotic mouse thymocytes, and the SYTO 16 stain (Cat. no. S7578) was found to be optimal for this application. The SYTO 16 stain has also been used with propidium iodide to differentiate live and dead COS-7 cells with a laser-based scanning cytometer.

The SYTO BC Green Fluorescent Nucleic Acid Stain is a mixture of some of our best SYTO dyes for bacterial staining and is a component of the Bacteria Counting Kit (Cat. No. B7277) for bacterial counting in flow cytometry.

The SYTO RNASelect Green Fluorescent Cell Stain is a cell-permeant nucleic acid stain that selectively stains RNA. Although virtually nonfluorescent in the absence of nucleic acids, the SYTO RNASelect stain exhibits bright green fluorescence when bound to RNA (absorption/emission maxima ∼490/530 nm), but only a weak fluorescent signal when bound to DNA. It has been used for staining RNA cargo in exosomes in both live cell samples and isolated exosomes.

SYTO Green Fluorescent Nucleic Acid Stain Sampler Kit

The SYTO Green Fluorescent Nucleic Acid Stain Sampler Kit #1 contains our collection of cell-permeant, green-fluorescent SYTO nucleic acid stains. Because the dyes may demonstrate different staining behaviors with various tissues and cells, it may be necessary to test the dyes to find the optimal dye for a specific application. The kit contains 50 μL each of SYTO 11–14, 16, 21, 24, and 25 dyes.

Any physiological buffer between pH 7.0–8.0, including PBS, can be used to dilute the SYTO dyes for the staining solution.

For Research Use Only. Not for use in diagnostic procedures.
사양
색상Green
농도5 mM solution in DMSO
검출 방법Fluorescence
염료 유형SYTO 14 Green
방출RNA: 549 nm, DNA: 547 nm
여기 파장 범위RNA: 517 nm, DNA: 521 nm
용도(애플리케이션)Fluorescent Labeling, Live Cell Imaging, Microarray
용도(장비)Fluorescence Microscope, High Content Imager, Flow Cytometer
제품라인SYTO
수량250 μL
배송 조건Room Temperature
보관 버퍼DMSO
부피(미터법)250 μL
라벨 유형Fluorescent Dye
제품 유형Nucleic Acid Stain
SubCellular LocalizationNucleic Acids
Unit SizeEach
구성 및 보관
Store in freezer at -5°C to -30°C and protect from light.

자주 묻는 질문(FAQ)

How do SYTO dyes bind to DNA?

The binding mode of SYTO nucleic acid stains is unknown. However, the behavior of these and related nucleic acid dyes suggests the following binding properties:

1.They appear to contact the solvent (suggested by sensitivity to salt, divalent cations, and in particular, SDS) and thus are likely to have contacts in the grooves.
2.All SYTO dyes appear to show some base selectivity and are thus likely to have minor groove contacts.
3.They can be removed from nucleic acid via ethanol precipitation; this characteristic is not shared by ethidium bromide and other intercalators. Likewise, the dyes are not removed from nucleic acid via butanol or chloroform extraction. These extraction methods do remove ethidium bromide from nucleic acid. 4. SYTO binding is not affected by nonionic detergents.
5. SYTO dyes are not quenched by BrdU, so they do not bind nucleic acids in precisely the same way as Hoechst 33342 and DAPI ((4′,6-diamidino-2-phenylindole).

SYBR Green I has shown little mutagenicity on frameshift indicator strains, indicating that it isn't likely to strongly intercalate.

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

인용 및 참조 문헌 (27)

인용 및 참조 문헌
Abstract
Translocation of RNA granules in living neurons.
Authors:Knowles RB, Sabry JH, Martone ME, Deerinck TJ, Ellisman MH, Bassell GJ, Kosik KS
Journal:J Neurosci
PubMed ID:8987809
'Sorting of RNAs to specific subcellular loci occurs in diverse settings from fly oocytes to mammalian neurons. Using the membrane-permeable nucleic acid stain SYTO 14, we directly visualized the translocation of endogenous RNA in living cells. Labeled RNA was distributed nonrandomly as discrete granules in neuronal processes. The labeled granules ... More
Nucleic acid dyes for detection of apoptosis in live cells.
Authors:Frey T
Journal:Cytometry
PubMed ID:8582249
'Apoptotic thymocytes were found to be much dimmer than normal thymocytes when stained with several nucleic acid dyes. These dyes provide a quick and simple assay for apoptosis which works for live cells and does not require a UV laser. The collection of dyes giving this staining pattern includes reagents ... More
A rapid sample preparation technique for flow cytometric analysis of immunofluorescence allowing absolute enumeration of cell subpopulations.
Authors:Terstappen LW, Meiners H, Loken MR
Journal:J Immunol Methods
PubMed ID:2477460
'A simple and rapid method was developed for immunofluorescence measurements of cells by flow cytometry which does not require washing procedures, permitting absolute enumeration of cell subpopulations. Peripheral blood cells were labeled with fluorescein and phycoerythrin conjugated monoclonal antibodies and the nucleic acid stain LDS-751. Distilled water was added following ... More
Neocentromere-mediated chromosome movement in maize.
Authors:Yu HG, Hiatt EN, Chan A, Sweeney M, Dawe RK
Journal:J Cell Biol
PubMed ID:9362502
'Neocentromere activity is a classic example of nonkinetochore chromosome movement. In maize, neocentromeres are induced by a gene or genes on Abnormal chromosome 10 (Ab10) which causes heterochromatic knobs to move poleward at meiotic anaphase. Here we describe experiments that test how neocentromere activity affects the function of linked centromere/kinetochores ... More
Disrupted-in-schizophrenia 1 regulates transport of ITPR1 mRNA for synaptic plasticity.
Authors:Tsuboi D, Kuroda K, Tanaka M, Namba T, Iizuka Y, Taya S, Shinoda T, Hikita T, Muraoka S, Iizuka M, Nimura A, Mizoguchi A, Shiina N, Sokabe M, Okano H, Mikoshiba K, Kaibuchi K
Journal:
PubMed ID:25821909
'Disrupted-in-schizophrenia 1 (DISC1) is a susceptibility gene for major psychiatric disorders, including schizophrenia. DISC1 has been implicated in neurodevelopment in relation to scaffolding signal complexes. Here we used proteomic analysis to screen for DISC1 interactors and identified several RNA-binding proteins, such as hematopoietic zinc finger (HZF), that act as components ... More