46945
Fluorescein isothiocyanate–dextran
average mol wt 70,000, (FITC:Glucose = 1:250)
Synonym(s):
FITC-Dextran 70, FITC–Dextran
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
biological source
synthetic
Quality Level
conjugate
FITC conjugate
form
powder
mol wt
average mol wt 70,000
composition
(FITC:Glucose = 1:250)
concentration
90-100 % (w/w) (TRITC DEXTRAN)
extent of labeling
~0.004 mol/mol FITC glucose
color
light orange to very dark orange, light yellow to very dark yellow
solubility
H2O: 50 mg/mL, hazy, orange to very deep orange
fluorescence
λex 492 nm; λem 518 nm in ethanol
application(s)
cell analysis
storage temp.
2-8°C
Application
Dextran labeled with fluorescein isothiocyanate for possible use in perfusion studies in animals.
Fluorescein isothiocyanate–dextran (FITC-Dextran 70) is use as a fluorescent probe to study cell processes such as cell permeability, phagocytosis and endocytosis and to study mechanisms of biomolecular delivery. FITC-Dextran 70 may be used to study the capacity, selectivity and efficiency of encapsulation and release by drug delivery vehicles.
Other Notes
Internalisation of FITC and FITC-dextran by suspension cultured plant cells; In the study of fluid pinocytosis in leukocytes
Still not finding the right product?
Explore all of our products under Fluorescein isothiocyanate–dextran
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
L. Cole et al.
Journal of Cell Science, 96, 721-721 (1990)
Use of horseradish peroxidase and fluorescent dextrans to study fluid pinocytosis in leukocytes.
J M Oliver et al.
Methods in enzymology, 108, 336-347 (1984-01-01)
Siegfried Weisenburger et al.
Cell, 177(4), 1050-1066 (2019-04-16)
Calcium imaging using two-photon scanning microscopy has become an essential tool in neuroscience. However, in its typical implementation, the tradeoffs between fields of view, acquisition speeds, and depth restrictions in scattering brain tissue pose severe limitations. Here, using an integrated
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 46945-100MG-F | 04061832358895 |
| 46945-500MG-F | 04061832358901 |