荧光
化学
生物物理学
共焦
荧光显微镜
亚历山福禄
分析化学(期刊)
钙
共焦显微镜
色谱法
生物
光学
细胞生物学
物理
有机化学
作者
Katrina Gee,K A Brown,W-N.U. Chen,Janell Bishop-Stewart,Diane R. Gray,Iain Johnson
出处
期刊:Cell Calcium
[Elsevier BV]
日期:2000-02-01
卷期号:27 (2): 97-106
被引量:599
标识
DOI:10.1054/ceca.1999.0095
摘要
We have developed fluo-4, a new fluorescent dye for quantifying cellular Ca2+ concentrations in the 100 nM to 1 microM range. Fluo-4 is similar in structure and spectral properties to the widely used fluorescent Ca(2+)-indicator dye, fluo-3, but it has certain advantages over fluo-3. Due to its greater absorption near 488 nm, fluo-4 offers substantially brighter fluorescence emission when used with excitation by argon-ion laser or other sources in conjunction with the standard fluorescein filter set. In vitro, fluo-4 exhibited high fluorescence emission, a high rate of cell permeation, and a large dynamic range for reporting [Ca2+] around a Kd(Ca2+) of 345 nM. We have also developed several Ca(2+)-indicators related to fluo-4 having lower affinities for Ca2+ that are useful in cellular studies requiring quantification of higher [Ca2+]. In a variety of physiological studies of live cells, fluo-4 labeled cells more brightly than did fluo-3, when challenged with procedures designed to elevate calcium levels. Fluo-4 is well suited for photometric and imaging applications that make use of confocal laser scanning microscopy, flow cytometry, or spectrofluorometry, or in fluorometric high-throughput microplate screening assays. Because of its higher fluorescence emission intensity, fluo-4 can be used at lower intracellular concentrations, making its use a less invasive practice.
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