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  Product  5 - FITC[5 - FITC;
  fluorescein - 5 - isothiocyanate]
  CAS  
  Size  1 g
  Catalog #  20151
  US$  127
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Description

Despite the availability of alternative amine-reactive fluorescein derivatives that yield conjugates with superior stability and comparable spectra, fluorescein isothiocyanate (FITC) remains one of the most popular fluorescent labeling reagents, probably due to the low cost of the material. 5-FITC and 6-FITC have very similar absorption and fluorescence spectra. However, the isomers may differ in their binding and reactivities to proteins, and the conjugates may elute under different chromatographic conditions or migrate differently in electrophoretic gels. Thus, we offer highly purified single isomers. It appears that 5-FITC is more widely used than the 6-FITC isomer. FITC reagents are prominently used to label proteins. In addition, FITC has also been used to label peptides, oligonucleotides and other small organic ligands. A collection of recent applications is listed in the following references.

Detailed Information Material Safety Data Sheets (MSDS)
Storage -20°C desiccated and protected from light
References Nakamura K, et al. (2002). The enhancing effect of nasal absorption of FITC-dextran 4,400 by beta- sitosterol beta-D-glucoside in rabbits. J Control Release 79, 147-55; Hattori S, et al. (2002). Real-time zymography and reverse zymography: a method for detecting activities of matrix metalloproteinases and their inhibitors using FITC- labeled collagen and casein as substrates. Anal Biochem 301, 27-34; Thiagarajah JR, et al. (2001). Evidence of amiloride-sensitive fluid absorption in rat descending colonic crypts from fluorescence recovery of FITC-labeled dextran after photobleaching. J Physiol 536, 541-53.
Molecular Weight 389.38
Molecular Formula C21H11NO5S
Spectral Properties Abs/Em = 494/519 nm
Solvent System DMSO
Product Citations Xia, W. et al. Proc Natl Acad Sci 104, 3841 (2007).
Li, M. et al. J Endocrinol 190, 313 (2006).


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