Di-2-ANEPEQ (JPW 1114)
Di-2-ANEPEQ (JPW 1114)
Invitrogen™

Di-2-ANEPEQ (JPW 1114)

ANEP dyes are molecules that fluoresce in response to electrical potential changes in their environment. These are fast-response probes that深入閱讀
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產品號碼Quantity
D6923
亦稱為 D-6923
5 mg
產品號碼 D6923
亦稱為 D-6923
價格 (TWD)
17,850.00
Online offer
Ends: 31-Dec-2025
25,500.00
您節省 7,650.00 (30%)
Each
新增至購物車
Quantity:
5 mg
價格 (TWD)
17,850.00
Online offer
Ends: 31-Dec-2025
25,500.00
您節省 7,650.00 (30%)
Each
新增至購物車
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:
• 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
• Cationic molecule; soluble in water (di-2-ANEPEQ is a water-soluble ANEP dye)
• Dye is typically introduced into cells by microinjection
• 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.
規格
Detection MethodFluorescence
Quantity5 mg
Shipping ConditionRoom Temperature
Sub Cellular LocalizationCell Membranes & Lipids
ColorInfrared
For Use With (Equipment)Fluorescence Microscope, Microplate Reader
Product TypeANEP Dye
Unit SizeEach
內容物與存放
Store at room temperature and protect from light.

常見問答集 (常見問題)

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.

引用資料與參考文獻 (26)

引用資料與參考文獻
Abstract
Dye screening and signal-to-noise ratio for retrogradely transported voltage-sensitive dyes.
Authors:Tsau Y, Wenner P, O'Donovan MJ, Cohen LB, Loew LM, Wuskell JP
Journal:J Neurosci Methods
PubMed ID:9007751
'Using a novel method for retrogradely labeling specific neuronal populations, we tested different styryl dyes in attempt to find dyes whose staining would be specific, rapid, and lead to large activity dependent signals. The dyes were injected into the ventral roots of the isolated chick spinal cord from embryos at ... More
Intrasarcomere [Ca2+] gradients and their spatio-temporal relation to Ca2+ sparks in rat cardiomyocytes.
Authors:Tanaka H, Sekine T, Kawanishi T, Nakamura R, Shigenobu K
Journal:J Physiol
PubMed ID:9490830
'1. Line-scan analyses of spontaneous Ca2+ sparks, non-propagating local rises in Ca2+ concentration, and the early phase of Ca2+ transients in cardiomyocytes were performed with a rapid-scanning laser confocal microscope (Nikon RCM8000) and fluo-3. 2. On electrical stimulation, points at which rise in Ca2+ began earliest were observed at regular ... More
Optical recording from cerebellar Purkinje cells using intracellularly injected voltage-sensitive dyes.
Authors:Kogan A, Ross WN, Zecevic D, Lasser-Ross N
Journal:Brain Res
PubMed ID:8624715
'We evaluated several techniques for their ability to record membrane potential changes with voltage-sensitive dyes introduced into CNS neurons in the brain slice preparation. Using a probe designed for intracellular application, JPW1114, we found that iontophoresis or pressure pulses could not push the lipophilic dye through electrodes whose resistance was ... More
Visual stimuli induce waves of electrical activity in turtle cortex.
Authors:Prechtl JC, Cohen LB, Pesaran B, Mitra PP, Kleinfeld D
Journal:Proc Natl Acad Sci U S A
PubMed ID:9207142
'The computations involved in the processing of a visual scene invariably involve the interactions among neurons throughout all of visual cortex. One hypothesis is that the timing of neuronal activity, as well as the amplitude of activity, provides a means to encode features of objects. The experimental data from studies ... More
Comparison of fluorescent voltage-sensitive dyes for multisite optical recording in hamster cerebral cortex by measurement of bicuculline-induced epileptiform events.
Authors:deBeer Zeiger J
Journal:Neuroimage
PubMed ID:9345545
'Two fluorescent voltage-sensitive dyes, RH795 and DI-2-ANEPPQ, were compared for in vivo multisite optical recording from the gustatory insular cortex of the golden Syrian hamster, the first reported use of DI-2-ANEPPQ in a mammalian brain preparation. The exposed cortex of the anesthetized hamster was stained with a 500 microM solution ... More