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Calcium is an important ubiquitous second messenger, involved in the regulation of a diverse range of cellular processes, including cell proliferation, gene transcription, muscle contraction and endocytosis. Calcium ions (Ca2+) from intracellular stores are released in response to adequate stimuli, increasing intracellular Ca2+ concentration, leading to activation, modulation and termination of cell function. Numerous pumps and channels allow this particular cation to enter and exit cells and move between the cytosol and intracellular stores.
We offer a large selection of probes for the detection of Ca2+ release, Ca2+ chelators and ionophores for the control of enzymatic activity regulated by Ca2+ signaling.
|Indicator||Excitation (nm)||Emission (nm)||Kd (nM)|
BAPTA is a non-fluorescent Ca2+ chelator which was derived from EGTA to give 105-fold selectivity for Ca2+ over Mg2+. It is commonly used in buffering and has a Kd of 160 nM in the absence of Mg2+. Also available in AM form.
Fura-2 is one of the first commercially available fluorescent calcium indicators. It exhibits excitation ratiometry at 340 nm/380 nm with emission at 505 nm. There are thousands of Fura-2 references in the scientific literature and it is one of most important Ca2+ indicator dyes to-date.
Indo-1 was introduced at the same time as Fura-2 in 1986. It is also ratiometric, but different in mode. Rather than being excitation ratiometric, it exhibits an emission ratio at 475 nm/405 nm when excited at 346 nm. Unlike Fura-2, it has a tendency to photobleach. It has also been used in a variety of applications, exemplified by the large number of literature publications.
Since its introduction in 1989, Fluo imaging has revealed the spatial dynamics of many elementary processes in Ca2+ signaling. Fluo-8 (or Fluo-2 Medium Affinity) has been found to be brighter (1.5x) than Fluo-4 in cellular experiments. It offers improved cell loading and Ca2+ response while maintaining the convenient Fluo-3 and Fluo-4 spectral wavelength of maximum excitation at 490 nm and maximum emission at 520 nm. Fluo-8 loading can be performed at room temperature.
Rhod-2, with fluorescence excitation maxima at 552 nm and emission maxima at 581 nm, was first introduced in 1989. Rhod-2 is essentially non-fluorescent before Ca2+ binding, becoming more fluorescent with increasing Ca2+ concentration. The longer excitations and emissions of Rhod-2 make the indicator useful for experiments in cells and tissues that have high levels of autofluorescence and for multiplexing with other fluorescent dyes of shorter wavelengths. The AM ester forms of these rhodamine-based indicators are cationic, which can result in potential-driven uptake into mitochondria.
A23187 (Calcimycin) has an intrinsic fluorescence excitable by UV light, making it less useful with UV-excitable Ca2+ indicators, e.g., Fura-2, but it is still useful for long-wavelength Ca2+ indicators, e.g., Fluo-2.
4-Bromo A-23187 is nonfluorescent and is thus compatible with all Ca2+ indicators. It is commonly used for in situ calibrations of fluorescent Ca2+ indicators, to equilibrate intracellular and extracellular Ca2+ concentrations and to permit Mn2+ to enter the cell to quench intracellular dye fluorescence.
Ionomycin is an effective Ca2+ ionophore that is commonly used to both calibrate fluorescent Ca2+ indicators and to modify intracellular Ca2+ concentrations and to when studying the regulatory properties of Ca2+ in cellular processes.