Fura-2 Am

Fura-2 AM is a membrane-permeant fluorescent calcium indicator used to measure intracellular calcium concentrations in living cells, including neurons. The acetoxymethyl ester form crosses the plasma membrane, where intracellular esterases cleave the ester groups and release charged Fura-2, trapping it inside the cell; calcium binding then changes its fluorescence according to excitation at approximately 340 and 380 nm, enabling ratiometric measurements. In neuroscience, Fura-2 AM helps visualize calcium influx and mobilization during neuronal stimulation, synaptic activity, and signaling. These measurements reveal changes in cellular excitability and calcium homeostasis while reducing sensitivity to variations in dye loading and illumination.

Fura-2 Am - Related Videos

Research

JoVE Journal - Biology

Calcium Imaging of Cortical Neurons using Fura-2 AM

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Cited by 108 •

2009

Calcium signals play a key role in many cellular processes including gene expression, survival and differentiation. Here we demonstrate how to perform calcium imaging using Fura-2 AM. Calcium imaging is a valuable tool to study the regulation of intracellular calcium in real time and its regulation of signaling cascades.

A Novel Nicotinamide Adenine Dinucleotide Correction Method for Intracellular Ca2+ Measurement with Fura-2-Analog in Live Cells

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2019

Due to the spectral overlapping of the excitation and emission wavelengths of NADH and fura-2 analogs, the signal interference from both chemicals in live cells is unavoidable during quantitative measurement of [Ca2+]. Thus, a novel online correction method of NADH signal interference to measure [Ca2+] was developed.

Assessment of Myofilament Ca2+ Sensitivity Underlying Cardiac Excitation-contraction Coupling

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Cited by 9 •

2016

This paper describes a protocol that assesses the changes of myofilament Ca2+ sensitivity during contraction in isolated cardiac myocytes from rat heart. Together with cardiac electrophysiology, systolic/diastolic cytosol Ca2+ levels and contraction/relaxation, this measurement is imperative in underpinning the mechanisms mediating cardiac excitation-contraction coupling in healthy and diseased hearts.

Education

JoVE Core - Organic Chemistry

meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H

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2023

All meta-directing substituents are deactivating groups. These substituents withdraw electrons from the aromatic ring, making the ring less reactive toward electrophilic substitution. For example, the nitration of nitrobenzene is 100,000 times slower than that of benzene because of the deactivating effect of the nitro group. The first step in an electrophilic aromatic substitution is the addition of an electrophile to form a resonance-stabilized carbocation. The energy diagrams for the...

2° Amines to N-Nitrosamines: Reaction with NaNO2

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2023

Secondary amines react with nitrous acid to form N-nitrosamines, as depicted in Figure 1. Nitrous acid, a weak and unstable acid, is formed in situ from an aqueous solution of sodium nitrite and strong acids, such as hydrochloric acid or sulfuric acid, in cold conditions. In the presence of an acid, the nitrous acid gets protonated. The subsequent loss of water results in the formation of the electrophile known as nitrosonium ion. Figure 1. The nitration reaction of secondary amines The...

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