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

SYTO赤色蛍光核酸染色サンプラーキットには、細胞透過性の赤色蛍光SYTO核酸染色試薬のコレクションが含まれています。色素はさまざまな組織や細胞で異なる染色挙動を示す可能性があるため、特定のアプリケーションに最適な色素を見つけるために色素をテストする必要がある場合があります。このキットには、SYTO17および59—64色素がそれぞれ50µL含まれています詳細を見る
製品番号(カタログ番号)数量
S113401 Kit
製品番号(カタログ番号) S11340
価格(JPY)
61,000
Online offer
Ends: 27-Mar-2026
101,700
割引額 40,700 (40%)
Each
お問い合わせください ›
数量:
1 Kit
SYTO赤色蛍光核酸染色サンプラーキットには、細胞透過性の赤色蛍光SYTO核酸染色試薬のコレクションが含まれています。色素はさまざまな組織や細胞で異なる染色挙動を示す可能性があるため、特定のアプリケーションに最適な色素を見つけるために色素をテストする必要がある場合があります。このキットには、SYTO17および59—64色素がそれぞれ50µL含まれています。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
Red
概要SYTO™ Red Fluorescent Nucleic Acid Stain Sampler Kit - SYTO™ dyes 17 and 59-64, 50 μL each
検出法蛍光
染色剤タイプ細胞透過性
発光634, 645, 678, 645, 676, 673, 619 nm
励起波長域621, 622, 652, 628, 652, 657, 599 nm
使用対象 (装置)蛍光顕微鏡、フローサイトメーター
製品ラインSYTO
数量1 Kit
出荷条件室温
容量(メートル法)50 μL
標識タイプFluorescent Dye
製品タイプStains Dimer Sampler Kit
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.

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

引用および参考文献 (3)

引用および参考文献
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