概要SYTO™ 17 Red Fluorescent Nucleic Acid Stain - 5 mM Solution in DMSO
検出法蛍光
染色剤タイプ細胞透過性
発光634 nm
励起波長域621⁄634
使用対象 (装置)蛍光顕微鏡
製品ラインSYTO
数量250 μL
出荷条件室温
容量(メートル法)250 μL
標識タイプFluorescent Dye
製品タイプ核酸染色
SubCellular Localization核酸
Unit SizeEach
組成および保存条件
フリーザー(-5℃~-30℃)に保存し、遮光してください。
よくあるご質問(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.
'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.
'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