SYTO™ Red Fluorescent Nucleic Acid Stain Sampler Kit - SYTO™ dyes 17 and 59-64 - 50 μL each
SYTO™ Red Fluorescent Nucleic Acid Stain Sampler Kit - SYTO™ dyes 17 and 59-64 - 50 μL each
Invitrogen™

SYTO™ Red Fluorescent Nucleic Acid Stain Sampler Kit - SYTO™ dyes 17 and 59-64 - 50 μL each

The SYTO Red Fluorescent Nucleic Acid Stain Sampler Kit contains our collection of cell-permeant, red-fluorescent SYTO nucleic acid stains. BecauseRead more
Catalog NumberQuantity
S113401 Kit
Catalog number S11340
Price (JPY)
61,000
온라인 행사
Ends: 27-Mar-2026
101,700
Save 40,700 (40%)
Each
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Quantity:
1 Kit

The SYTO Red Fluorescent Nucleic Acid Stain Sampler Kit contains our collection of cell-permeant, red-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 17 and 59–64 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.
Specifications
ColorRed
DescriptionSYTO™ Red Fluorescent Nucleic Acid Stain Sampler Kit - SYTO™ dyes 17 and 59-64, 50 μL each
Detection MethodFluorescence
Dye TypeCell-Permeant
Emission634, 645, 678, 645, 676, 673, 619 nm
Excitation Wavelength Range621, 622, 652, 628, 652, 657, 599 nm
For Use With (Equipment)Fluorescence Microscope
Product LineSYTO
Quantity1 Kit
Shipping ConditionRoom Temperature
Volume (Metric)50 μL
Label TypeFluorescent Dye
Product TypeStains Dimer Sampler Kit
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 (3)

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
Novel model for multispecies biofilms that uses rigid gas-permeable lenses.
Authors:Peyyala R, Kirakodu SS, Ebersole JL, Novak KF,
Journal:Appl Environ Microbiol
PubMed ID:21421785
Oral biofilms comprise complex multispecies consortia aided by specific inter- and intraspecies interactions occurring among commensals and pathogenic bacterial species. Oral biofilms are primary initiating factors of periodontal disease, although complex multifactorial biological influences, including host cell responses, contribute to the individual outcome of the disease. To provide a system ... More