SYTO™ 61 Red Fluorescent Nucleic Acid Stain - 5 mM Solution in DMSO
SYTO™ 61 Red Fluorescent Nucleic Acid Stain - 5 mM Solution in DMSO
Invitrogen™

SYTO™ 61 Red Fluorescent Nucleic Acid Stain - 5 mM Solution in DMSO

細胞透過性SYTO61赤色蛍光核酸色素は、核酸に結合すると明るい赤色の蛍光を示します。生細胞におけるSYTO色素の染色パターンは細胞タイプによって異なる場合があるため、当社はSYTO Red Fluorescent Nucleic Acid Stain Sampler詳細を見る
製品番号(カタログ番号)数量
S11343250 μL
製品番号(カタログ番号) S11343
価格(JPY)
74,100
Each
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数量:
250 μL

細胞透過性SYTO61赤色蛍光核酸色素は、核酸に結合すると明るい赤色の蛍光を示します。生細胞におけるSYTO色素の染色パターンは細胞タイプによって異なる場合があるため、当社はSYTO Red Fluorescent Nucleic Acid Stain Sampler Kit(カタログ番号S-11340)を提供しています。これを使用することで、研究者は使用している系に最適な赤色蛍光SYTO色素を見つけることができます。

染色液用にSYTO色素を希する際は、PBSなどのpH 7.0~8.0の生理的バッファーを使用できます。

研究用途にのみご使用ください。診断目的には使用できません。
仕様
赤色
概要SYTO™ 61 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645 nm
励起波長域628 nm
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
標識タイプ蛍光
製品タイプ核酸染色
SubCellular Localization核酸
Unit SizeEach
組成および保存条件
-5℃~-30℃のフリーザーで保存し、遮光する。

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 (17)

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
Modulation of [Ca2+]i signaling dynamics and metabolism by perinuclear mitochondria in mouse parotid acinar cells.
Authors:Bruce JI, Giovannucci DR, Blinder G, Shuttleworth TJ, Yule DI
Journal:J Biol Chem
PubMed ID:14699167
'Parotid acinar cells exhibit rapid cytosolic calcium signals ([Ca2+]i) that initiate in the apical region but rapidly become global in nature. These characteristic [Ca2+]i signals are important for effective fluid secretion, which critically depends on a synchronized activation of spatially separated ion fluxes. Apically restricted [Ca2+]i signals were never observed ... More
An evaluation of the performance of cDNA microarrays for detecting changes in global mRNA expression.
Authors:Yue H, Eastman PS, Wang BB, Minor J, Doctolero MH, Nuttall RL, Stack R, Becker JW, Montgomery JR, Vainer M, Johnston R
Journal:Nucleic Acids Res
PubMed ID:11292855
'The cDNA microarray is one technological approach that has the potential to accurately measure changes in global mRNA expression levels. We report an assessment of an optimized cDNA microarray platform to generate accurate, precise and reliable data consistent with the objective of using microarrays as an acquisition platform to populate ... More
Differentiation of Phytophthora infestans sporangia from other airborne biological particles by flow cytometry.
Authors:Day JP, Kell DB, Griffith GW
Journal:Appl Environ Microbiol
PubMed ID:11772606
'The ability of two different flow cytometers, the Microcyte (Optoflow) and the PAS-III (Partec), to differentiate sporangia of the late-blight pathogen Phytophthora infestans from other potential airborne particles was compared. With the PAS-III, light scatter and intrinsic fluorescence parameters could be used to differentiate sporangia from conidia of Alternaria or ... More
The use of fluorescence enhancement to improve the microscopic diagnosis of falciparum malaria.
Authors:Guy R, Liu P, Pennefather P, Crandall I,
Journal:Malar J
PubMed ID:17617912
'BACKGROUND: Giemsa staining of thick blood smears remains the "gold standard" for detecting malaria. However, this method is not very good for diagnosing low-level infections. A method for the simultaneous staining of Plasmodium-parasitized culture and blood smears for both bright field and fluorescence was developed and its ability to improve ... More