What is fura Red?
Fura Red is a visible light-excitable fura-2 analog that offers unique possibilities for ratiometric measurement of calcium ion in single cells by microphotometry, imaging or flow cytometry when used with single excitation, green-fluorescent calcium indicators.
How does Fura-2 work?
Fura-2, an aminopolycarboxylic acid, is a ratiometric fluorescent dye which binds to free intracellular calcium. The use of the ratio automatically cancels out confounding variables, such as variable dye concentration and cell thickness, making Fura-2 one of the most appreciated tools to quantify calcium levels.
What is calcium flux?
Indo-1 is the ratio metric calcium indicator dye most commonly used in flow cytometry because of its shift in emission frequency when excited at a single wavelength. …
Why is Fura-2 unable to cross cell membranes?
Calcium indicators are unable to cross lipid membranes due to their nature, making necessary the use of physical or chemical methods to load them inside the cell. This is the case of Indo-1 AM and Fura-2 AM, which are fluorescent and calcium insensitive. …
What is a Fura-2 ratio?
Fura-2 is a ratiometric and sensitive indicator dye for measuring intracellular calcium. At low concentrations of the indicator, 340/380 nm excitation ratio for fura-2 allows accurate measurements of the intracellular Ca2+ concentration (Figure 1).
What is a calcium flux assay?
Calcium Flux Assay Kit (Flow cytometry) (ab233472) is a fluorescence-based assay for detecting intracellular calcium mobilization using a flow cytometer. It can be used for kinetic reading or for endpoint reading.
What is Flipr?
FLIPR (Fluorescent Imaging Plate Reader) was developed to perform quantitative optical screening for cell-based kinetic assays. FLIPR incorporates an integrated design, including low-level optical detection, precise temperature control, and precise fluid handling, all in one package.
What is 2 photon calcium imaging?
Two-photon calcium imaging is a powerful means for monitoring the activity of distinct neurons in brain tissue in vivo. In vivo two-photon Ca2+ recordings, obtained by imaging through the intact skull, indicated that whisker deflection-evoked Ca2+ transients occur in a subset of layer 2/3 neurons of the barrel cortex.