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FURA-2 AM (ultra pure)

Calcium dye
 
ENZ-52006 1 mg 200.00 USD
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Replaces Prod. #: ALX-620-005

Fura-2 acetomethoxy (AM) is one of the most widely used calcium indicators for homogenous quantitative dual wavelength ratiometric cell measurements. Fura-2 AM is particularly useful for digital imaging microscopy. It is less susceptible to photobleaching than Indo-1. The probe is excited only by UV light, which results in significantly less interference by visible wavelength excitable fluorescent compounds. One application of the probe is as a useful counter screen tool for GPCR and calcium channel hits identified using calcium indicators excited at 488nm in primary screens. Fura-2 AM can be easily loaded into cells by passive incubation. Wavelength Maxima: Excitation 370nm, Emission 476nm

Product Details

Alternative Name:1-[2-(5-Carboxyoxazol-2-yl)-6-aminobenzofuran-5-oxy]-2-(2'-amino-5'-methyl-phenoxy)ethane-N,N,N',N'-tetraacetic acid, pentaacetoxymethyl ester
 
Formula:C44H47N3O24
 
MW:1001.9
 
CAS:108964-32-5
 
Purity:≥95% (HPLC)
 
Appearance:Off-white to yellow solid.
 
Solubility:Soluble in DMSO.
 
Shipping:Ambient Temperature
 
Long Term Storage:-20°C
 
Use/Stability:Stable for at least one year after receipt when stored as recommended.
 
Handling:Protect from light. Keep cool and dry.
 
Technical Info/Product Notes:This product is a member of the CELLESTIAL® product line, reagents and assay kits comprising fluorescent molecular probes that have been extensively benchmarked for live cell analysis applications. CELLESTIAL® reagents and kits are optimal for use in demanding imaging applications, such as confocal microscopy, flow cytometry and HCS, where consistency and reproducibility are required.
 
Regulatory Status:RUO - Research Use Only
 
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Product Literature References

TRPM3 Is Expressed in Afferent Bladder Neurons and Is Upregulated during Bladder Inflammation: M. Vanneste, et al.; Int. J. Mol. Sci. 23, 107 (2022), Abstract;
Measurement of [Ca2+]i in whole cell suspensions using fura-2: R.A. Hirst, et al.; Methods Mol. Biol. 312, 37 (2006), Abstract;
Two-photon microscopy of fura-2-loaded cardiac myocytes with an all-solid-state tunable and visible femtosecond laser source: G. McConnell, et al.; Opt. Lett. 28, 1742 (2003), Abstract;

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