JC-9 Dye (Mitochondrial Membrane Potential Probe)
JC-9 Dye (Mitochondrial Membrane Potential Probe)
Invitrogen™

JC-9 Dye (Mitochondrial Membrane Potential Probe)

La sonda de potencial de membrana mitocondrial radiométrica JC-9 muestra fluorescencia verde que es independiente del potencial de membrana yMás información
Have Questions?
Número de catálogoCantidad
D224215 mg
Número de catálogo D22421
Precio (USD)
929,88
Each
Añadir al carro de la compra
Cantidad:
5 mg
Precio (USD)
929,88
Each
Añadir al carro de la compra
La sonda de potencial de membrana mitocondrial radiométrica JC-9 muestra fluorescencia verde que es independiente del potencial de membrana y un aumento en la fluorescencia roja en potenciales de membrana hiperpolarizados.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Método de detecciónFluorescente
Cantidad5 mg
Condiciones de envíoTemperatura ambiente
Localización subcelularMitocondrias
ColorVerde
Para utilizar con (equipo)Microscopio de fluorescencia, Citómetro de flujo
Tipo de productoSonda de potencial de membrana mitocondrial
Unit SizeEach
Contenido y almacenamiento
Almacenar a temperatura ambiente y proteger de la luz.

Preguntas frecuentes

I am seeing high background outside of my neuronal cells when using membrane potential indicators. What can I do to reduce background?

If you use our FluoVolt Membrane Potential Kit (Cat. No. F10488), the kit provides a background suppressor to reduce this problem. For other indicators, consider the use of BackDrop Background Suppressor (Cat no. R37603, B10511, and B10512).

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

What is the difference between fast and slow-response membrane potential probes?

Molecules that change their structure in response to the surrounding electric field can function as fast-response probes for the detection of transient (millisecond) potential changes. Slow-response dyes function by entering depolarized cells and binding to proteins or membranes. Increased depolarization results in additional dye influx and an increase in fluorescence, while hyperpolarization is indicated by a decrease in fluorescence. Fast-response probes are commonly used to image electrical activity from intact heart tissues or measure membrane potential changes in response to pharmacological stimuli. Slow-responding probes are often used to explore mitochondrial function and cell viability.

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

What type of membrane potential indicators do you offer and how should I choose one for my experiment?

A membrane potential indicator selection guide can be found here (https://www.thermofisher.com/us/en/home/life-science/cell-analysis/cell-viability-and-regulation/ion-indicators/membrane-potential-indicators.html).

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

Citations & References (5)

Citations & References
Abstract
Synthesis and identification of small molecules that potently induce apoptosis in melanoma cells through G1 cell cycle arrest.
Authors:Dothager RS, Putt KS, Allen BJ, Leslie BJ, Nesterenko V, Hergenrother PJ,
Journal:J Am Chem Soc
PubMed ID:15954774
'Late-stage malignant melanoma is a cancer that is refractory to current chemotherapeutic treatments. The average survival time for patients with such a diagnosis is 6 months. In general, the vast majority of anticancer drugs operate through induction of cell cycle arrest and cell death in either the DNA synthesis (S) ... More
Chlorophenols and chlorocatechols induce apoptosis in human lymphocytes (in vitro).
Authors:Michalowicz J, Sicinska P,
Journal:Toxicol Lett
PubMed ID:19766705
In this work the effect of 2,4,5-trichlorophenol (2,4,5-TCP), pentachlorophenol (PCP), 4,6-dichloroguaiacol (4,6-DCG), tetrachloroguaiacol (TeCG), 4,5-dichlorocatechol (4,5-DCC) and tetrachlorocatechol (TeCC) on the induction of apoptosis in human peripheral blood lymphocytes was examined. The analysis of the changes in mitochondrial transmembrane potential (DeltaPsi(m)) was performed using JC-9 fluorescent probe. It was noted ... More
Markers of apoptosis: methods for elucidating the mechanism of apoptotic cell death from the nervous system.
Authors:Smyth PG, Berman SA,
Journal:Biotechniques
PubMed ID:11911667
Apoptosis is a highly conserved energy-requiring program for non-inflammatory cell death that is important in both normal physiology and disease. Numerous techniques have been used to study apoptosis. In the nervous system, apoptosis is necessary for normal development, but it also occurs in many acute and chronic pathologic conditions. This ... More
DGAT1-Dependent Lipid Droplet Biogenesis Protects Mitochondrial Function during Starvation-Induced Autophagy.
Authors:
Journal:Dev Cell
PubMed ID:28697336
A role for mitochondria in the establishment and maintenance of the maize root quiescent center.
Authors:
Journal:Plant Physiol
PubMed ID:16443698