FURA-2AM
Tocris Bioscience | Catalog # 2220
Key Product Details
Description
Wavelength
Product Description
FURA-2AM is a fluorescent ratiometric Ca2+ indicator (Kd Ca2+ = 145 nM). FURA-2AM is selective for Ca2+ over other divalent cations Mg2+, Zn2+, Fe2+ and Mn2+. FURA-2AM binds to free intracellular calcium and is used to determine [Ca2+]i concentration.
This product is typically prepared in DMSO. F 127 (Cat. No. 6253) for the solubilization of FURA-2AM is also available.
Optical Data
| λabs | 371 nm |
| λem | 474 nm |
| Extinction Coefficient (ε) | 30000 M-1cm-1 |
| Cell Permeable | Yes |
| Application | Flow Cytometry, Fluorescent Microscopy |
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Product Specifications for FURA-2AM
Molecular Weight
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Chemical Name
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PubChem ID
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The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
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Background References
References are publications that support the biological activity of the product. See our Citations tab to view 9 publications citing the usage of this product.
- Wang Sildenafil inhibits human pulmonary artery smooth muscle cell proliferation by decreasing capacitative Ca2+ entry. J.Pharmacol.Sci. 2008 PMID: 18818482
- Grynkiewicz A new generation of Ca2+ indicators with greatly improved fluorescence properties. J.Biol.Chem. 1985 PMID: 3838314
Product Documents for FURA-2AM
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for FURA-2AM
For research use only
Citations for FURA-2AM
Customer Reviews for FURA-2AM (3)
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Customer Images
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Species: RatAssay Type: In VitroCell Line/Tissue: RBL-2H3Verified Customer | Posted 11/02/2018RBL-2H3 cells at a confluency of 50–60% were cultured on glass coverslip and loaded with 2 μM Fura-2AM 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. The Fura-2 loaded cells were excited alternately at 340 and 380 nm and fluorescence was captured at 510 nm every 1.2 s. 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: Guinea PigAssay Type: In VitroCell Line/Tissue: primary ventricular cardiomyocytesVerified Customer | Posted 10/15/2018Primary guinea pig ventricular cardiomyocytes were loaded with FURA-2AM (1 μM) and Pluronic F 127 (1%) for 30 min followed by washing with normal-Tyrode solution. Cells were stimulated at 1 Hz frequency and fluorescence intensities were measured.
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Species: RatAssay Type: In VitroCell Line/Tissue: spinal cord neuronsVerified Customer | Posted 11/01/2017Used in live cell calcium imaging assay to study glutamate receptor signaling in neurons. Used at a concentration of 5 micromolar (along with pluronic). Images shows changes in fura-2 fluorescence pre (left) and post(right) glutamate stimulation.
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