Fluo-4 AM
Tocris Bioscience | Catalog # 6255
Key Product Details
Description
Wavelength
Product Description
Fluo-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.
Optical Data
| 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 |
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Product Specifications for Fluo-4 AM
Molecular Weight
Formula
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Chemical Name
CAS Number
PubChem ID
InChI Key
SMILES
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 23 publications citing the usage of this product.
- Gee Chemical and physiological characterization of fluo-4 Ca2+-indicator dyes. Cell Calcium. 2000 PMID: 10756976
Product Documents for Fluo-4 AM
Certificate of Analysis
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Product Specific Notices for Fluo-4 AM
For research use only
Citations for Fluo-4 AM
Customer Reviews for Fluo-4 AM (2)
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Customer Images
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Species: RatAssay Type: In VitroCell Line/Tissue: RBL-2H3Verified Customer | Posted 12/24/2019RBL-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+.
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Species: RatAssay Type: In VitroCell Line/Tissue: motor neuronsVerified Customer | Posted 10/24/2018motor 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.Used for imaging calcium entry in motor neurons at 1 mM concentration
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