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GFP (FL3) Antibody DB088 0.100 mg/ml $300.00

Datasheet 
Datasheet 

For technical service please call (800) 595 1994
Product Info
Background 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) 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). 
Origin Rabbits were immunized with highly purified green-fluorescent protein (GFP) isolated directly from Aequorea victoria. Antibodies were affinity purified using the native GFP immobilized on a solid phase. 
Product Details Each vial contains 100 µg/ml of affinity purified rabbit IgG, GFP DB088 (FL3), in 1 ml PBS containing 0.1 % sodium azide and 0.2% gelatin. 
Form 100 µg/ml rabbit polyclonal IgG in 1 ml PBS containing 0.1 % sodium azide and 0.2% gelatin. 
Immunogen Highly purified green-fluorescent protein (GFP) isolated directly from Aequorea victoria. 
Specificity DB088 GFP (FL3) recognizes all variants of recombinant Aequorea green-fluorescent protein. 
Use ELISA, Western blotting, immunoprecitation, and immunhistochemistry. Suggested working dilutions: Elisa: 1:10,000-1:100,000, western blotting: 1:1,000-1:5,000. 
Storage Store this product at 4º C, do not freeze. The product is stable for one year from the date of shipment. 
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.
 

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