SYTO™ 17 Red Fluorescent Nucleic Acid Stain - 5 mM Solution in DMSO
SYTO™ 17 Red Fluorescent Nucleic Acid Stain - 5 mM Solution in DMSO
Invitrogen™

SYTO™ 17 Red Fluorescent Nucleic Acid Stain - 5 mM Solution in DMSO

The cell-permeant SYTO 17 red fluorescent nucleic acid stain exhibits bright, red fluorescence upon binding to nucleic acids. Because theRead more
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Catalog NumberQuantity
S7579250 μL
Catalog number S7579
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3,515.00
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Quantity:
250 μL
Price (CNY)
3,515.00
Online Exclusive
Ends: 31-Dec-2025
4,765.00
Save 1,250.00 (26%)
Each
Add to cart

The cell-permeant SYTO 17 red fluorescent nucleic acid stain exhibits bright, red fluorescence upon binding to nucleic acids. Because the staining pattern of the SYTO dyes in live cells may vary between cell types, we offer the SYTO Red Fluorescent Nucleic Acid Stain Sampler Kit (Cat. No. S-11340) to enable researchers to find the most appropriate red-fluorescent SYTO stain for their system.

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.
Specifications
ColorRed
DescriptionSYTO™ 17 Red Fluorescent Nucleic Acid Stain - 5 mM Solution in DMSO
Detection MethodFluorescence
Dye TypeCell-Permeant
Emission634 nm
Excitation Wavelength Range621 nm
For Use With (Equipment)Fluorescence Microscope
Product LineSYTO
Quantity250 μL
Shipping ConditionRoom Temperature
Volume (Metric)250 μL
Label TypeFluorescent Dye
Product TypeNucleic Acid Stain
SubCellular LocalizationNucleic Acids
Unit SizeEach
Contents & Storage
Store in freezer at -5°C to -30°C and protect from light.

Frequently asked questions (FAQs)

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.

Citations & References (22)

Citations & References
Abstract
Multiparameter detection of apoptosis using red-excitable SYTO probes.
Authors:Wlodkowic D, Skommer J, Hillier C, Darzynkiewicz Z,
Journal:Cytometry A
PubMed ID:18431792
'Functional assays allowing phenotypic characterization of different cell death parameters at a single-cell level are important tools for preclinical anticancer drug screening. Currently, the selection of cytometric assays is limited by the availability of fluorescent probes with overlapping spectral characteristics. Following on our earlier reports on green and orange fluorescent ... More
Liver fatty acid-binding protein colocalizes with peroxisome proliferator activated receptor alpha and enhances ligand distribution to nuclei of living cells.
Authors:Huang H, Starodub O, McIntosh A, Atshaves BP, Woldegiorgis G, Kier AB, Schroeder F
Journal:Biochemistry
PubMed ID:14992586
'Although it is hypothesized that long-chain fatty acyl CoAs (LCFA-CoAs) and long-chain fatty acids (LCFAs) regulate transcription in the nucleus, little is known regarding factors that determine the distribution of these ligands to nuclei of living cells. Immunofluorescence colocalization showed that liver fatty acid-binding protein (L-FABP; binds LCFA-CoA as well ... More
Confocal laser scanning microscopy of urinary bladder after intravesical instillation of a fluorescent dye.
Authors:Koenig F, Knittel J, Schnieder L, George M, Lein M, Schnorr D
Journal:Urology
PubMed ID:12837458
'OBJECTIVES: To assess the potential of confocal laser scanning microscopy for imaging of the urinary bladder after intravesical instillation of a fluorescent dye. METHODS: The study was performed on the bladder of male Copenhagen rats. For confocal fluorescence microscopy (CFM), a standard confocal laser scanning microscope (Zeiss LSM 410) was ... More
Induction of DNA damage response by the supravital probes of nucleic acids.
Authors:Zhao H, Traganos F, Dobrucki J, Wlodkowic D, Darzynkiewicz Z,
Journal:Cytometry A
PubMed ID:19373929
'The aim of this study was to assess the potential DNA damage response (DDR) to four supravitally used biomarkers Hoechst 33342 (Ho 42), DRAQ5, DyeCycle Violet (DCV), and SYTO 17. A549 cells were exposed to these biomarkers at concentrations generally applied to live cells and their effect on histone H2AX ... More
Fiber cell denucleation in the primate lens.
Authors:Bassnett S
Journal:Invest Ophthalmol Vis Sci
PubMed ID:9286256
'PURPOSE: To determine the morphologic and biochemical events preceding the breakdown of fiber cell nuclei in the primate lens. METHODS: Monkey lens slices were labeled with fluorescent probes and optically sectioned using a confocal microscope. The distribution of nuclear histones was visualized by immunofluorescence. DNA and cellular membranes were imaged ... More