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Adipogen/Fluorescein diacetate/CDX-F0027-G010/10 g

  
  2025-11-05
  
More Information Product Details Synonyms Product Type Properties Formula MW CAS Source/Host Chemicals Purity Chemicals Appearance Solubility Identity Declaration Other Product Data InChi Key Shipping and Handling Shipping Short Term Storage Long Term Storage Handling Advice Use/Stability Documents MSDS Product Specification Sheet Datasheet
FDA; 3,6-Diacetoxyfluoran; Di-O-Acetylfluorescein; Cellstain-FDA; NSC 4726; NSC 667259
Chemical
C24H16O7
416.38
596-09-8
Synthetic.
≥95% (NMR)
White to off-white powder.
Soluble in DMSO, ethanol, water, chloroform or acetone (25mg/ml).
Determined by 1H-NMR.
Manufactured by Chemodex.
Click here for Original Manufacturer Product DatasheetOur product description may differ slightly from the original manufacturers product datasheet.
CHADEQDQBURGHL-UHFFFAOYSA-N
AMBIENT
+4°C
-20°C
Keep cool and dry.Protect from light and moisture.
Stable for at least 2 years after receipt when stored at -20°C.
No
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FDA is a non-fluorescent hydrophobic fluorescein derivative that can pass through the cell membrane whereupon intracellular esterases hydrolyze the diacetate group producing the highly fluorescent product fluorescein. The fluorescein molecules accumulate in cells that possess intact membranes so the green fluorescence can be used as a marker of cell viability. Cells that do not possess an intact cell membrane or an active metabolism may not accumulate the fluorescent product and therefore do not exhibit green fluorescence. FDA may be used in combination with PI staining as the non-viable cells take up the PI and stain dead cells red whereas viable cells do not take up the PI and should only stain green. This 2-color separation of non-viable and viable cells may provide a more accurate quantitation of cell viability than single color analysis. FDA is used in studies on intracellular interactions and membrane permeability, for flow cytometry and as esterase substrate. Spectral data: λex=494nm, λem=521nm.

Product References

(1) B. Rotman, et al.; PNAS 55, 134 (1966) | (2) H.R. Hulett, et al.; Science 166, 747 (1969) | (3) K.H. Jones, et al.; J. Histochem. Cytochem. 33, 77 (1985) | (4) K. McGinnes, et al.; J. Immunol. Methods 86, 7 (1986) | (5) D.D. Ross, et al.; Cancer Res. 49, 3776 (1989) | (6) E. Prosperi; Histochem. J. 22, 227 (1990) | (7) M. Miyamoto, et al.; Cell Transplant 9, 681 (2000) | (8) S. Wanandy, et al.; J. Microbiol. Methods 60, 21 (2005) | (9) J. Wang, et al.; Drug Metab. Dispos. 39, 1329 (2011) | (10) N. Saruyama, et al.; Anal. Biochem. 441, 58 (2013)

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