Di-4-ANEPPDHQ
Di-4-ANEPPDHQ
Invitrogen™

Di-4-ANEPPDHQ

ANEP dyes are molecules that fluoresce in response to electrical potential changes in their environment. These are fast-response probes thatRead more
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Catalog NumberQuantity
D368021 mg
Catalog number D36802
Price (CLP)
786.381
Each
Add to cart
Quantity:
1 mg
Price (CLP)
786.381
Each
Add to cart
ANEP dyes are molecules that fluoresce in response to electrical potential changes in their environment. These are fast-response probes that operate by means of a change in their electronic structure, and consequently their fluorescence properties, in response to a change in the surrounding electric field. Their optical response is sufficiently fast to detect transient (millisecond) potential changes in excitable cells, including single neurons, cardiac cells, and intact brains. However, the magnitude of their potential-dependent fluorescence change is often small; fast-response probes typically show a 2-10% fluorescence change per 100 mV. Furthermore, these dyes display a potential-dependent shift in their excitation spectra, thus permitting the quantitation of membrane potential using excitation ratio measurements.

Learn more about ion indicators including calcium, potassium, pH, and membrane potential indicators ›

Potential-Sensitive ANEP Dye Specifications:
• Cationic molecule; exhibits very low internalization and good signal:noise ratio and is useful for visualizing cholesterol-enriched lipid domains in model membranes
• Ex/Em maxima bound to model phospholipid membranes are ∼465/635 nm (but spectral properties are highly dependent on environment)
• Nonfluorescent until bound to membranes
• Soluble in ethanol, DMSO, and DMF (di-2-ANEPEQ is a water-soluble ANEP dye)
• Dye is introduced into cells by direct addition of stock solution to cell culture medium, by using Pluronic™ F-127, or by retrograde labeling
• Fast-response probe, suitable for detecting submillisecond membrane potential changes


Applications for Potentiometric Probes
The plasma membrane of a cell typically has a transmembrane potential of approximately -70 mV (negative inside) as a consequence of K+, Na+, and Cl- concentration gradients that are maintained by active transport processes. Potentiometric probes offer an indirect method of detecting the translocation of these ions.

Increases and decreases in membrane potential-referred to as membrane hyperpolarization and depolarization, respectively-play a central role in many physiological processes, including nerve-impulse propagation, muscle contraction, cell signaling and ion-channel gating. Potentiometric probes are important tools for studying these processes.

Find More ANEP Dyes
We offer ANEP dyes in various forms. Review Fast-Response Probes-Section 22.2 in the Molecular Probes™ Handbook for more information on these probes.

For Research Use Only. Not for human or animal therapeutic or diagnostic use.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Detection MethodFluorescence
Quantity1 mg
Shipping ConditionRoom Temperature
Sub Cellular LocalizationCytoplasm & Cytosol
ColorInfrared
For Use With (Equipment)Fluorescence Microscope
Product TypeANEP Dye
Unit SizeEach
Contents & Storage
Store in freezer -5°C to -30°C and protect from light.

Frequently asked questions (FAQs)

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 (15)

Citations & References
Abstract
Novel naphthylstyryl-pyridium potentiometric dyes offer advantages for neural network analysis.
Authors:Obaid AL, Loew LM, Wuskell JP, Salzberg BM
Journal:J Neurosci Methods
PubMed ID:15003384
'The submucous plexus of the guinea pig intestine is a quasi-two-dimensional mammalian neural network that is particularly amenable to study using multiple site optical recording of transmembrane voltage (MSORTV) [Biol. Bull. 183 (1992) 344; J. Neurosci. 19 (1999) 3073]. For several years the potentiometric dye of choice for monitoring the ... More
Cholesterol-enriched lipid domains can be visualized by di-4-ANEPPDHQ with linear and nonlinear optics.
Authors:Jin L, Millard AC, Wuskell JP, Clark HA, Loew LM
Journal:Biophys J
PubMed ID:15879475
We present a membrane-staining dye, di-4-ANEPPDHQ, which differentiates liquid-ordered phases from liquid-disordered phases coexisting in model membranes under both linear and nonlinear microscopies. The dye's fluorescence emission spectrum is blue-shifted 60 nm in liquid-ordered phases compared with liquid-disordered phases, and shows strong second harmonic generation in the liquid-disordered phase compared ... More
Spectral characterization of the voltage-sensitive dye di-4-ANEPPDHQ applied to probing live primary and immortalized neurons.
Authors:Wang Y, Jing G, Perry S, Bartoli F, Tatic-Lucic S,
Journal:Opt Express
PubMed ID:19158915
Spectral properties of a recently developed voltage-sensitive dye, di-4-ANEPPDHQ, were characterized as the dye was dissolved in the solvent dimethyl sulfoxide as the stock solution, in Hank's buffered salt solution as the staining solution, and bound to the plasma membrane of primary rat hippocampal neurons and immortalized mouse hypothalamic neurons ... More
Laurdan and di-4-ANEPPDHQ do not respond to membrane-inserted peptides and are good probes for lipid packing.
Authors:Dinic J, Biverståhl H, Mäler L, Parmryd I,
Journal:Biochim Biophys Acta
PubMed ID:20937246
Laurdan and di-4-ANEPPDHQ are used as probes for membrane order, with a blue shift in emission for membranes in liquid-ordered (lo) phase relative to membranes in liquid-disordered (ld) phase. Their use as membrane order probes requires that their spectral shifts are unaffected by membrane proteins, which we have examined by ... More
Characterization and application of a new optical probe for membrane lipid domains.
Authors:Jin L, Millard AC, Wuskell JP, Dong X, Wu D, Clark HA, Loew LM
Journal:Biophys J
PubMed ID:16415047
In this article, we characterize the fluorescence of an environmentally sensitive probe for lipid membranes, di-4-ANEPPDHQ. In large unilamellar lipid vesicles (LUVs), its emission spectrum shifts up to 30 nm to the blue with increasing cholesterol concentration. Independently, it displays a comparable blue shift in liquid-ordered relative to liquid-disordered phases. ... More