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1 h a fluorescent intracellular calcium probe: Fura-2 AM.
2 , and [Ca2+]i transients were evaluated with Fura-2 AM.
3 rge-scale activity was imaged optically with fura-2 AM.
4 tracellular calcium ([Ca2+]i) kinetics using fura-2 AM.
5 fluorospectrometry using the fluorescent dye Fura-2/AM.
6 ng an imaging system in acini incubated with fura-2/AM.
7 t, when IgG preparations were incubated with fura-2-AM (acetyloxymethyl ester)-loaded human keratinoc
8 were independently measured with the use of fura 2-AM and 4,5-diaminofluorescein diacetate (DAF-2DA)
9 n ASM cells loaded with the Ca(2+) indicator fura 2-AM and imaged using fluorescence microscopy, we e
11 rmined with the ratiometric Ca(2+) indicator fura-2 AM and was similar in mutant and control boutons
12 broblasts were loaded with the calcium probe Fura-2/AM and exposed to a single 3-min pulse of 100 mic
13 Bovine trachealis cells were loaded with fura 2-AM, and cytosolic calcium concentrations ([Ca2+]i
14 changes in cytosolic calcium ([Ca2+]i) using fura 2-AM (fluorescence at 340/380 nm) during perfusion
15 tion mediated by ET-1 was measured using the Fura-2 AM fluorescent probe technique as an index of ET
16 ient in rat sensory neurons was tested using fura-2 AM imaging and electrophysiological recordings.
17 root ganglion (DRG) neurons, the loading of Fura-2 AM is often facilitated by the use of pluronic F-
18 onitoring fluxes in Ca2+ concentration using Fura 2-AM-loaded PMN, and 3) degranulation using an MPO
19 lcium concentration ([Ca2+]i) was studied in fura-2 AM-loaded equine tracheal myocytes at 35 degrees
21 and intracellular calcium was determined in Fura-2 AM-loaded, electrical field-paced cardiomyocytes.
22 ippocampal neurones in culture coloaded with fura-2 AM or fura-2FF AM and rhodamine 123 (Rh 123).
23 cardiomyocyte [Ca2+]i and [Na+]i measured by fura-2-AM or sodium-binding benzofurzan isophthalate loa
25 of thapsigargin-evoked current changes with fura-2/AM results from separate cells indicated that bot
26 lar recordings using the calcium-imaging dye fura-2 AM revealed that GABA or muscimol triggered a sus
27 ng studies using fura-2 acetoxymethyl ester (fura-2 AM) revealed that the increase in intracellular f
28 tes were loaded with the fluorescent reagent fura 2/AM to measure intracellular free calcium ([Ca2+]i
29 issociated rat glomus cells were loaded with Fura-2 AM to study the effects of hypoxia, and carotid b
33 Using the conventional calcium indicator, fura-2/AM, we estimated [Ca2+]i elevations to be approxi
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