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Questions? Please consult our answers to frequently asked questions at http://www.ebioscience.com/faq. DescriptionThis is a peptide mapping near the carboxy terminus of Aequorea victoria GFP. Green fluorescent protein was originally cloned from the cnidarian, Aequorea victoria. This exceptional protein absorbs blue light (maximally at 395 nm) and emits green light (peak at 509 nm) without the requirement of exogenous substrates and cofactors (1). These unique qualities allow GFP to be used to monitor gene expression and protein localization in vivo. Several mutant forms of GFP have been developed which fluoresce more intensely and have shifted excitation maxima when compared to the wild type GFP, making them useful for FACS, fluorescence microscopy, and double-labeling applications (2,3). Applications ReportedFor research use only, not for diagnostic or therapeutic use. This blocking peptide has been reported for use in competition studies. References
1. Chalfie M, Tu Y., Euskirchen G., Ward W.W., Prasher D.C. 1994. Green Fluorescent Protein as a Marker for Gene Expression. Science 263: 802-805. 2. Cormack B.P., Valdivia R.H., and Falkow S. 1996. FACS-optimized mutants of the green fluorescent protein (GFP). Gene 173: 33-38. 3. Rizzuto R., Brini M., De Giorgi F., Rossi R., Heim R., Tsien R.Y., and Pozzan T. 1996. Double labelling of the subcellular structures with organelle-targeted GFP mutants in vivo. Curr.Biol. 6:183-188. Related ProductsCat. 14-6758 Purified Anti-GFP and GFP mutant fusion proteins polyclonal (clone Polyclonal) |
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