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Submit ReviewFluo-4 AM is a cell-permeable, fluorescent Ca2+ indicator (Kd Ca2+ = 345 nM). Displays no resting signal and 100-fold increase in emission intensity upon Ca2+ binding. Excitation/emission λ 494/506 nm.
It is recommended to prepare stock solutions in DMSO.
Emission Color | Green |
---|---|
λabs | 494 nm |
λem | 506 nm |
Closest Laser line | 488 nm |
Cell Permeable | Yes |
Application | Fluorescence Microscopy, Flow Cytometry, Fluorometric Microplate Reading Assays |
Use our spectra viewer to interactively plan your experiments, assessing multiplexing options. View the excitation and emission spectra for our fluorescent dye range and other commonly used dyes.
Spectral Viewer分子量 | 1096.95 |
公式 | C51H50F2N2O23 |
储存 | Store at -20°C |
纯度 | ≥95% (HPLC) |
CAS Number | 273221-67-3 |
PubChem ID | 4060965 |
InChI Key | QOMNQGZXFYNBNG-UHFFFAOYSA-N |
Smiles | O=C(C(F)=C1)C=C2C1=C(C3=CC=C(N(CC(OCOC(C)=O)=O)CC(OCOC(C)=O)=O)C(OCCOC4=CC(C)=CC=C4N(CC(OCOC(C)=O)=O)CC(OCOC(C)=O)=O)=C3)C5=CC(F)=C(OCOC(C)=O)C=C5O2 |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
参考文献是支持产品生物活性的出版物。
Gee et al (2000) Chemical and physiological characterization of fluo-4 Ca2+-indicator dyes. Cell Calcium. 27 97 PMID: 10756976
If you know of a relevant reference for Fluo-4 AM, please let us know.
关键词: Fluo-4 AM, Fluo-4 AM supplier, Fluo-4AM, Fluo-4, cell, permeable, calcium, Ca2+, indicator, fluorescent, Ion, Indicators, General, Calcium, Signaling, Agents, Fluorescent, 6255, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 Fluo-4 AM 的部分引用包括:
Gerald W et al (2022) Norepinephrine transporter defects lead to sympathetic hyperactivity in Familial Dysautonomia models. Nat Commun 13 7032 PMID: 36396637
Bernardo et al (2020) Heterosynaptic Plasticity Determines the Set Point for Cortical Excitatory-Inhibitory Balance. Neuron 106 842-854.e4 PMID: 32213321
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平均评分: 4.5 (基于 2 条评论。)
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RBL-2H3 cells cultured on glass coverslip were loaded with 2 μM Fluo-4AM in normal tyrode solution (NT) for 40 min at room temperature in the dark. Then, the cells were washed twice and left to equilibrate for at least 20 min in NT. Fluo-4-loaded cells were excited at 490 nm and fluorescence was captured at 510 nm every 2.4 s and normalized to the initial value. ER Ca2+ store was depleted with 500 nM thapsigargin which promotes store-operated Ca2+ entry into the cells upon addition of 2 mM extracellular Ca2+.
Used for imaging calcium entry in motor neurons at 1 mM concentration
motor neurons loaded with 1 mM concentration of fluo4-am loaded at 37 degrees for 15 minutes in aCSF. After 15 minutes cells were gently washed with aCSF twice and left in dark for 10 minutes for complete de-esterification of the dye.
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