Vybrant™ CFDA SE Cell Tracer Kit
Vybrant™ CFDA SE Cell Tracer Kit
Invitrogen™

Vybrant™ CFDA SE Cell Tracer Kit

El kit de marcaje celular Vybrant™ CFDA SE se utiliza en análisis fluorescentes como un marcador de células a largoMás información
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Número de catálogoCantidad
V128831 kit
Número de catálogo V12883
Precio (MXN)
-
Cantidad:
1 kit
El kit de marcaje celular Vybrant™ CFDA SE se utiliza en análisis fluorescentes como un marcador de células a largo plazo. Este método se utiliza comúnmente para el etiquetado in vitro e in vivo de las células para determinar si una célula está proliferando o no.

• Rendimiento superior: permite una tinción brillante y uniforme de las células
• Retención a largo plazo: el colorante se conserva bien en las células durante varios días tras la tinción
• No tóxico: mínima citotoxicidad para ensayos in vivo e in vitro
• Protocolo de tinción simple y sólido

Tinción fluorescente superior
El etiquetado exitoso de las células requiere un colorante extremadamente brillante para distinguir las células etiquetadas con fluorescencia de la autofluorescencia. La intensa tinción fluorescente que proporciona el kit de etiquetado celular Vybrant™ CFDA SE permite la visualización de células etiquetadas durante varios días después de la tinción, lo que la convierte en una tinción ideal para estudios de marcado celular basados en la dilución de colorante.

Retención de señal a largo plazo
El colorante Vybrant™ CFDA SE cruza fácilmente la membrana plasmática y se une covalentemente dentro de las células, donde el colorante fluorescente estable y bien conservado está diseñado para proporcionar una señal consistente, incluso después de varios días en un entorno de cultivo celular.

No tóxico
El colorante Vybrant™ CFDA SE se une covalentemente a todas las aminas libres en la superficie y el interior de las células y muestra poca citotoxicidad, con un efecto mínimo observado en la capacidad proliferativa o biología de las células. Los investigadores han utilizado el etiquetado CFDA SE para demostrar que las células hematopoyéticas transplantables proliferan in vitro en respuesta a la estimulación mediante un cóctel de factores de crecimiento.

Protocolo de tinción simple y sólido
El kit de etiquetado celular Vybrant™ CFDA SE contiene viales prácticos y de un solo uso de colorante seco para permitir realizar experimentos a pequeña escala sin preparar cantidades excesivas de colorante, lo que prolonga la vida útil del colorante no disuelto en la solución. Se prepara una solución madre mediante la disolución del contenido de un vial en dimetilsulfóxido (DMSO) anhidro antes del uso. Para teñir 1 ml de células en un medio sin proteínas, se suele emplear 1 µl de esta solución madre. Las células deben teñirse durante 20 minutos a temperatura ambiente mediante una agitación suave. A continuación, un breve lavado con un medio completo eliminará cualquier coorante que pudiera quedar en la solución.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Método de detecciónFluorescente
Tipo de coloranteCFDA SE (CFSE)
Intervalo de longitud de onda de excitación492⁄517
Para utilizar con (equipo)Microscopio de fluorescencia, citómetro de flujo
FormularioSólido
FormatoTubos, portaobjetos
Línea de productosVybrant
Cantidad1 kit
Condiciones de envíoTemperatura ambiente
SolubilidadDMSO (dimetilsulfóxido)
Tipo de etiquetaOtras etiquetas o colorantes
Tipo de productoKit de marcaje celular CFDA SE
Unit Size1 kit
Contenido y almacenamiento
Contiene 10 viales de 5(6)-CFDA, SE (CFSE, 500 μg por vial) y 1 vial de DMSO (1,3 ml). Almacenar en congelador (de – 5 a – 30 °C).

Preguntas frecuentes

I'm trying to label my cells in suspension and track them over time by labeling with CFDA SE, but after labeling them they will no longer adhere to a surface (whereas unlabeled cells adhere well). I've tried to label at 10 and 20 µM. What is causing this?

This dye will bind to proteins via primary amines. Too high of a concentration can lead to cell toxicity or unintended modification of cell function. The solution is to reduce the concentration and/or staining time, or to go with a non-protein-binding tracking reagent, such as Qtracker cell labeling reagents.

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

I want to do a cell migration study for around 4 hours and need to fluorescently label the cells with a dye. What do you recommend?

Calcein, AM and FDA (fluorescein diaceate) are examples of some dyes used for this application. Since these dyes are not incorporated or covalently attached to any cellular components, they may have a short retention time as some cell types may actively efflux the dye out of the cells. The CellTracker and CellTrace dyes include either a mild thiol-reactive chloromethyl group or amine-reactive succinnimidyl ester group to allow for covalent binding to cellular components, providing for better retention. As with any reagent, one should empirically determine retention times for the cell type used.

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

I labeled my cells with Calcein, AM, but when I imaged the next day, there was no fluorescence from Calcein. Why?

Calcein, AM is a good choice for cell tracking and as a general cytoplasmic stain. However, it doesn't bind to anything and may be actively pumped out of the cells within a couple hours, which is likely what happened. The retention of Calcein within live cells is dependent upon the inherent properties of the cell type and culture conditions.

For long-term imaging, you may wish to consider a reactive cytoplasmic stains such as CFDA, SE or the CellTracker and CellTrace dyes.

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

I want to track my cells with a nucleic acid stain, like DAPI or Hoechst dye. Do you recommend this?

This is not recommended. When these stains bind to DNA and RNA, they may affect the normal function of the nucleic acids, disrupting transcription, as well as replication. Other reagents, such as CellTracker dyes or Qtracker reagents are more optimized for tracking without disrupting normal activity. If a nuclear label is still desired, though, and the cells are mammalian and non-hematopoietic, CellLight nuclear reagents can transiently transfect cells to express GFP or RFP on a nuclear-expressing protein for up to several days without affecting function.

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

I want to track my cells over time, and you have a lot of options to choose from. How do I pick the right one?

Please see this Web link (http://www.thermofisher.com/us/en/home/life-science/cell-analysis/cell-tracing-tracking-and-morphology/cell-tracking.html) to help you choose the right option for your application. Start by planning how long you want to track your cells, then consider the mechanism of binding. Calcein dyes are very uniform in label and are good for short-term cell migration, but may be rapidly effluxed from some cell types. Lipophilic cyanine dyes, such as DiI, DiO, and similar dyes label cell membranes, don’t disrupt function, and can last longer, but have the potential to cross to other cells if membranes fuse. They are also lost upon permeabilization. CellTracker dyes are better for longer-term labeling, as they possess a mildly reactive chloromethyl moiety that allows covalent binding to cellular components. CFDA SE also covalently binds to cellular components. With all the reagents, their retention within cells is dependent upon the rate of cell division and the inherent properties of the cell (active efflux, membrane and protein turnover rates, etc.) and reagents that allow for covalent attachment exhibit longer retention than those that do not.

The longest-lasting and brightest options are the Qtracker reagents, which are taken up through endocytosis. These are so bright individual quantum dots can be detected, and are also robust enough to survive not only fixation and permeabilization, but even the heat and solvents used in paraffin processing.

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

Citations & References (477)

Citations & References
Abstract
Fas/Fas ligand interactions promote activation-induced cell death of NK T lymphocytes.
Authors:Leite-de-Moraes MC,Herbelin A,Gouarin C,Koezuka Y,Schneider E,Dy M
Journal:Journal of immunology (Baltimore, Md. : 1950)
PubMed ID:11035073
Phenotypic and functional effects of heat shock protein 90 inhibition on dendritic cell.
Authors:Bae J,Mitsiades C,Tai YT,Bertheau R,Shammas M,Batchu RB,Li C,Catley L,Prabhala R,Anderson KC,Munshi NC
Journal:Journal of immunology (Baltimore, Md. : 1950)
PubMed ID:17548610
Calcein: a novel marker for lymphocytes which enter lymph nodes.
Authors:Weston SA, Parish CR
Journal:Cytometry
PubMed ID:1451604
Previous studies have identified unique cell surface antigens which are associated with the specific binding of lymphocytes to high endothelial venules (HEV). Evidence is presented in this paper which demonstrates that uptake of the fluorescent dye calcein by lymphocytes represents an additional marker for the lymph node homing subpopulation of ... More
Platelet-endothelial interaction in tumor angiogenesis and microcirculation.
Authors:Manegold PC, Hutter J, Pahernik SA, Messmer K, Dellian M
Journal:Blood
PubMed ID:12584142
Activated platelets release angiogenic growth factors and have therefore been proposed to contribute to tumor angiogenesis within a potentially prothrombotic tumor microcirculation. The aim of the study was to investigate interactions of platelets with the angiogenic microvascular endothelium of highly vascularized solid tumors during growth and in response to endothelial ... More
Primitive, quiescent, Philadelphia-positive stem cells from patients with chronic myeloid leukemia are insensitive to STI571 in vitro.
Authors:Graham SM, Jørgensen HG, Allan E, Pearson C, Alcorn MJ, Richmond L, Holyoake TL
Journal:Blood
PubMed ID:11756187
In clinical trials, the tyrosine kinase inhibitor STI571 has proven highly effective in reducing leukemic cell burden in chronic myeloid leukemia (CML). The overall sensitivity of CML CD34(+) progenitor cells to STI571 and the degree to which cell death was dependent on cell cycle status were determined. Stem cells (Lin(-)CD34(+)) ... More