CellROX™ Orange Flow Cytometry Assay Kit
CellROX™ Orange Flow Cytometry Assay Kit
Invitrogen™

CellROX™ Orange Flow Cytometry Assay Kit

Das CellROX™ Orange Flow Cytometry Assay Kit ermöglicht die durchflusszytometrische Erkennung von reaktiven Sauerstoffspezies (ROS) in lebenden Zellen. Das KitWeitere Informationen
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KatalognummerMenge
C10493100 Assays
Katalognummer C10493
Preis (EUR)
424,65
Exklusiv online
483,00
Ersparnis 58,35 (12%)
Each
Zum Warenkorb hinzufügen
Menge:
100 Assays
Preis (EUR)
424,65
Exklusiv online
483,00
Ersparnis 58,35 (12%)
Each
Zum Warenkorb hinzufügen
Das CellROX™ Orange Flow Cytometry Assay Kit ermöglicht die durchflusszytometrische Erkennung von reaktiven Sauerstoffspezies (ROS) in lebenden Zellen. Das Kit enthält das neuartige fluorogene CellROX™ Orange Reagenz sowie SYTOX™ Red Totzellen-Farbstoff, N-Acetylcystein (Antioxidans, für negative Kontrolle) und tert-Butylhydroperoxid-Lösung (TBHP, ein Induktor von ROS).

Auswahlhilfe für alle CellROX™ Reagenzien und Kitsanzeigen.

Das CellROX™ Orange Durchflusszytometrie-Assay-Kit bietet:

• Für Durchflusszytometrie konzipierte fluorogene Sonde, die in Anwesenheit von ROS oxidiert
• Mehrfarb-Kompatibilität – minimale Überlappung mit Fluorophoren, die durch andere Laserlinien angeregt werden, ermöglicht einfaches Multiplexing mit anderen Reagenzien
• Einfaches Protokoll – Zellen können in kompletten Medien oder einem anderen geeigneten Puffer gefärbt werden, kein serumfreies Medium erforderlich

Das CellROX™ Orange Detektionsreagenz ist zelldurchlässig und im reduzierten Zustand nicht-fluoreszierend oder sehr schwach fluoreszierend. Bei Oxidation zeigt das Reagenz eine starkes Fluoreszenzsignal mit einem Absorptions-/Emissionsmaximum von 545/565 nm und verbleibt im Zytoplasma. Bei Verwendung zusammen mit dem im Lieferumfang enthaltenen SYTOX™ Red Dead Cell Stain werden oxidativ gestresste und nicht gestresste Zellen mittels Durchflusszytometrie zuverlässig von toten Zellen unterschieden.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
FormatTube
Menge100 Assays
Excitation/EmissionCellROX Orange: 545/565, SYTOX Red: 640/658
Unit SizeEach

Häufig gestellte Fragen (FAQ)

What dyes can I use to detect reactive oxygen species (ROS) in my bacteria?

Many dyes that are used on mammalian cells have also been shown to be useful in bacterial cells. For example, CellROX Deep Red Reagent has been shown to work in B. subtilis (see Reference: http://www-brs.ub.ruhr-uni-bochum.de/netahtml/HSS/Diss/RaatschenNadja/diss.pdf). If you are interested in a particular dye, but are not sure if it will work on your bacteria, literature searches are the best way to check to see if it has been tested. If not, then it may be worth testing yourself.

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

What cellular processes can be analyzed with a flow cytometer?

-Calcium flux: Each of the Oregon Green calcium indicators binds intracellular calcium with increasing affinity, providing a sensitivity range to match many applications. Oregon Green probes emit green fluorescence at resting levels of Ca2+ and increase their fluorescence intensity 14-fold with increasing Ca2+ concentration. The cell-permeant formulation (Cat. No. O6807) can be loaded in cell media and is compatible with flow cytometry.
-Rhodamine-based calcium indicators comprise a range of probes for large or small changes in Ca2+ concentration. They exhibit a 50-fold increase in fluorescence upon calcium binding and offer a range of wavelengths that can be used in conjunction with GFP or green-fluorescent dyes for multiplexing. Rhod-2, AM (Cat. No. R1245MP), in particular, localizes to mitochondria and can be used with flow cytometry.
-Membrane potential: A distinctive feature of the early stages of apoptosis is the disruption of the mitochondria, including changes in membrane and redox potential. We offer a range of products specifically designed to assay mitochondrial membrane potential in live cells by flow cytometry, with minimal disruption of cellular function. The MitoProbe family of mitochondrial stains (Cat. Nos. M34150, M34151, and M34152) provide quick, easy, and reliable flow cytometric detection of the loss of mitochondrial membrane potential that occurs during apoptosis. MitoTracker dyes (Cat. Nos. M7510 and M7512) are membrane potential-dependent probes for staining mitochondria in live cells. The staining pattern of MitoTracker dyes is retained throughout subsequent flow cytometry immunocytochemistry, DNA end labeling, in situ hybridization, or counterstaining steps. The Mitochondrial Permeability Transition Pore Assay (Cat. No. M34153) provides a more direct method of measuring mitochondrial permeability transition pore opening than assays relying on mitochondrial membrane potential alone. The mitochondrial permeability transition pore (MPTP) is a non-specific channel formed by components from the inner and outer mitochondrial membranes, and appears to be involved in the release of mitochondrial components during cell death.
-Phagocytosis: In phagocytosis, cells internalize particulate matter such as microorganisms, and this process is important for immune responses and during the clearance of apoptotic cells. Probes for studying phagocytosis include BioParticles indicators—bacteria and yeast labeled with fluorescent dyes.
-Tracking phagocytosis using a quench/wash-based assay can report on simple uptake, or a pH indicator can be used to monitor stages in the pathway. We have no-wash assays labeled with pHrodo Red or Green (Cat. Nos. A10010, P35361, P35364, P35365, P35366, and P35367) and no-wash assays for whole blood (Cat. Nos. A10025, A10026, P35381, and P35382), all suitable for flow cytometry.
-pH changes: Sensitive pH determinations can be made in a physiological range using either fluorescent intensity or ratiometric measurements. pHrodo dyes (Cat. Nos. P35373 and P35372) provide signal intensity modulation from pH 2 to pH 9 and with a choice of fluorescent wavelengths. Tracking internalization of fluorescent dextran is a routine method for analyzing pH changes in cellular compartments. Dextran conjugates of pHrodo dyes (Cat. Nos. P35368 and P10361) provide the most complete solution by allowing discrimination of vesicles from early endosomes to lysosomes, with no quench or wash required.
-Reactive oxygen species: Cells that are environmentally stressed usually contain greatly increased levels of reactive oxygen species (ROS). CellROX reagents are fluorogenic probes developed for the detection and quantitation of ROS in live cells. These cell-permeant reagents are non-fluorescent or very weakly fluorescent in the reduced state; however, when oxidized, they become brightly fluorescent and remain localized within the cell. We offer CellROX Green (Cat. No. C10492), CellROX Orange (Cat. No. C10493), and CellROX Deep Red (Cat. No. C10491) Assay Kits validated for flow cytometry.

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

Zitierungen und Referenzen (11)

Zitierungen und Referenzen
Abstract
Fluorescent probes for the detection of reactive oxygen species in human spermatozoa.
Authors:Escada-Rebelo S, Mora FG, Sousa AP, Almeida-Santos T, Paiva A, Ramalho-Santos J
Journal:
PubMed ID:31939350
'Reactive oxygen species (ROS) production is a by-product of mitochondrial activity and is necessary for the acquisition of the capacitated state, a requirement for functional spermatozoa. However, an increase in oxidative stress, due to an abnormal production of ROS, has been shown to be related to loss of sperm function, ... More
MicroRNA-27 (miR-27) Targets Prohibitin and Impairs Adipocyte Differentiation and Mitochondrial Function in Human Adipose-derived Stem Cells.
Authors:Kang T, Lu W, Xu W, Anderson L, Bacanamwo M, Thompson W, Chen YE, Liu D,
Journal:
PubMed ID:24133204
Prohibitin (PHB) has been reported to play a crucial role in adipocyte differentiation and mitochondrial function. However, the regulative mechanism of PHB during adipogenesis remains unclear. In this study, we determined that the levels of both microRNA (miR)-27a and miR-27b were down-regulated following adipogenic induction of human adipose-derived stem cells, ... More
Hypoxia and IF1 Expression Promote ROS Decrease in Cancer Cells.
Authors:Sgarbi G, Gorini G, Liuzzi F, Solaini G, Baracca A
Journal:Cells
PubMed ID:29933600
'The role of reactive oxygen species (ROS) in the metabolic reprogramming of cells adapted to hypoxia and the interplay between ROS and hypoxia in malignancy is under debate. Here, we examined how ROS levels are modulated by hypoxia in human cancer compared to untransformed cells. Short time exposure (20 min) ... More
Isolation of strawberry anthocyanin-rich fractions and their mechanisms of action against murine breast cancer cell lines.
Authors:Mazzoni L, Giampieri F, Alvarez Suarez JM, Gasparrini M, Mezzetti B, Forbes Hernandez TY, Battino MA
Journal:Food Funct
PubMed ID:31621765
'The aim of this study was the evaluation of the effects of strawberry anthocyanin extract treatment on two in vitro models of murine breast cancer cell lines, in an attempt to detect a specific pathway (AMP-activated protein kinase or AMPK) through which strawberries exert their anticancer activity. The anticancer activity ... More
Berberine Effects on NF?B, HIF1A and NFE2L2/AP-1 Pathways in HeLa Cells.
Authors:Belanova A, Beseda D, Chmykhalo V, Stepanova A, Belousova M, Khrenkova V, Gavalas N, Zolotukhin P
Journal:Anticancer Agents Med Chem
PubMed ID:30526471
'Berberine has multitudinous anti-cancer stem cells effects making it a highly promising candidate substance for the next-generation cancer therapy. However, berberine modes of action predispose it to significant side-effects that probably limit its clinical testing and application.' ... More