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

The cell-permeant SYTO 61 red fluorescent nucleic acid stain exhibits bright, red fluorescence upon binding to nucleic acids. Because the자세히 알아보기
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카탈로그 번호수량
S11343250 μL
카탈로그 번호 S11343
제품 가격(KRW)
434,000
온라인 행사
Ends: 31-Dec-2025
510,000
할인액 76,000 (15%)
Each
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수량:
250 μL
제품 가격(KRW)
434,000
온라인 행사
Ends: 31-Dec-2025
510,000
할인액 76,000 (15%)
Each
카트에 추가하기

The cell-permeant SYTO 61 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.
사양
색상Red
설명SYTO™ 61 Red Fluorescent Nucleic Acid Stain - 5 mM Solution in DMSO
검출 방법Fluorescence
염료 유형Cell-Permeant
방출645 nm
여기 파장 범위628 nm
용도(장비)Fluorescence Microscope
제품라인SYTO
수량250 μL
배송 조건Room Temperature
부피(미터법)250 μL
라벨 유형Fluorescent Dye
제품 유형Nucleic Acid Stain
SubCellular LocalizationNucleic Acids
Unit SizeEach
구성 및 보관
Store in freezer at -5°C to -30°C and protect from light.

자주 묻는 질문(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.

인용 및 참조 문헌 (17)

인용 및 참조 문헌
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