SYTOX™ Orange Nukleinsäurefärbemittel – 5 mmol-Lösung in DMSO
SYTOX™ Orange Nukleinsäurefärbemittel – 5 mmol-Lösung in DMSO
Invitrogen™

SYTOX™ Orange Nukleinsäurefärbemittel – 5 mmol-Lösung in DMSO

SYTOX Orange färbt Nukleinsäuren in Zellen mit kompromittierten Membranen. Diese Färbung ist als Indikator für den Zelltod nützlich und vielWeitere Informationen
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KatalognummerMenge
S11368250 μl
Katalognummer S11368
Preis (EUR)
426,24
Sonderangebot
Exklusiv online
Endet: 15-Mar-2026
576,00
Ersparnis 149,76 (26%)
Each
Zum Warenkorb hinzufügen
Menge:
250 μl
Preis (EUR)
426,24
Sonderangebot
Exklusiv online
Endet: 15-Mar-2026
576,00
Ersparnis 149,76 (26%)
Each
Zum Warenkorb hinzufügen
SYTOX Orange färbt Nukleinsäuren in Zellen mit kompromittierten Membranen. Diese Färbung ist als Indikator für den Zelltod nützlich und viel heller als Propidiumiodid (P-1304).
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
FarbeOrange
NachweisverfahrenFluoreszenz, Fluoreszent
FarbstofftypMembrangängig
Emission570 nm
Anregungswellenlängenbereich547 nm
Zur Verwendung mit (Geräte)Fluoreszenzmikroskop, Durchflusszytometer
FormLösung
FormatRöhrchen, Röhrchen
ProduktlinieSYTOX
Menge250 μl
VersandbedingungRaumtemperatur, Raumtemperatur
Volumen (metrisch)250 μl
MarkertypFluoreszent
ProdukttypNukleinsäurefärbemittel
SubCellular LocalizationNukleinsäuren
Unit SizeEach
Inhalt und Lagerung
Enthält 1 Fläschchen mit SYTOX™ orange Nukleinsäure-Farbstoff (5 mmol Lösung in DMSO)

Im Tiefkühlschrank (-5 bis -30 °C), trocken und vor geschützt Licht lagern.

Häufig gestellte Fragen (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.

Zitierungen und Referenzen (41)

Zitierungen und Referenzen
Abstract
Nucleosomes are exposed at the cell surface in apoptosis.
Authors:Radic M, Marion T, Monestier M
Journal:J Immunol
PubMed ID:15153485
'Apoptotic cells are considered the source of DNA, histones, and nucleoprotein complexes that drive the production of autoantibodies in systemic lupus erythematosus. However, the role of apoptotic cells in the activation of the immune system is not clear. To explore interactions that may initiate or sustain the production of anti-nuclear ... More
Peroxisome proliferator-activated receptor gamma-mediated regulation of neural stem cell proliferation and differentiation.
Authors:Wada K, Nakajima A, Katayama K, Kudo C, Shibuya A, Kubota N, Terauchi Y, Tachibana M, Miyoshi H, Kamisaki Y, Mayumi T, Kadowaki T, Blumberg RS
Journal:J Biol Chem
PubMed ID:16524877
'Peroxisome proliferator-activated receptor gamma (PPARgamma) plays an important role in insulin sensitivity, tissue homeostasis, and regulating cellular functions. We found high-level expression of PPARgamma in embryo mouse brain and neural stem cells (NSCs), in contrast to extremely low levels in adult mouse brain. Here, we show that PPARgamma mediates the ... More
Diverse microglial motility behaviors during clearance of dead cells in hippocampal slices.
Authors:Petersen MA, Dailey ME
Journal:Glia
PubMed ID:15042586
'We used two-channel three-dimensional time-lapse fluorescence confocal imaging in live rat hippocampal slice cultures (1-7 days in vitro) to determine the motility behaviors of activated microglia as they engage dead and dying cells following traumatic brain tissue injury. Live microglia were labeled with a fluorescently conjugated lectin (IB(4)), and dead ... More
Probing the kinetics of SYTOX Orange stain binding to double-stranded DNA with implications for DNA analysis.
Authors:Yan X, Habbersett RC, Yoshida TM, Nolan JP, Jett JH, Marrone BL
Journal:Anal Chem
PubMed ID:15924389
'Rapid binding kinetics of SYTOX Orange stain with double-stranded DNA (dsDNA) was revealed on the DNA fragment sizing flow cytometer. We demonstrated for the first time that the dye molecules could be adsorbed onto the capillary surface and native DNA fragments can be dynamically stained while passing through the capillary. ... More
Droplet microfluidic technology for single-cell high-throughput screening.
Authors:Brouzes E, Medkova M, Savenelli N, Marran D, Twardowski M, Hutchison JB, Rothberg JM, Link DR, Perrimon N, Samuels ML,
Journal:Proc Natl Acad Sci U S A
PubMed ID:19617544
'We present a droplet-based microfluidic technology that enables high-throughput screening of single mammalian cells. This integrated platform allows for the encapsulation of single cells and reagents in independent aqueous microdroplets (1 pL to 10 nL volumes) dispersed in an immiscible carrier oil and enables the digital manipulation of these reactors ... More