WebGFP is a fluorescent protein that can be expressed in vivo. If GFP is exposed to light, it emits a green fluorescent signal. This property has had an enormous impact on cell biology by enabling the imaging of almost any protein, in transcription studies by working as a reporter gene, and in biochemical applications. 2. Origin of GFP WebPrasher's GFP work was funded by the National Cancer Institute. In his grant he suggested that it should be possible to take the GFP gene out of the jellyfish cell and attach it to cancer cells so that they would be …
THE GREEN FLUORESCENT PROTEIN - University of California, …
WebPrimary structure of the Aequorea victoria green-fluorescent protein. Gene 111: 229-233 (1992). Original report on the characterization of GFP from Aequorea victoria (referred to as gfp10 ), which encodes a 238-amino acid polypeptide with a calculated molecular weight of 26,888. The authors suggest that the gfp gene is comprised of at least ... WebFeb 23, 2009 · The GFP gene was first inserted into the genome of potato virus X, a plant pathogen. One to two days after inoculation of the recombinant virus onto plants, regions of the leaves fluoresced bright … imprimerie montfort monthey
Removal of a cryptic intron and subcellular localization of green ...
Douglas C. Prasher (born August 1951) is an American molecular biologist. He is known for his work to clone and sequence the genes for the photoprotein aequorin and green fluorescent protein (GFP) and for his proposal to use GFP as a tracer molecule. He communicated his pioneering work to Martin Chalfie and Roger Y. Tsien, but by 1991 was himself unable to obtain further research funding, and left academia. Eventually, he had to abandon science. Chalfie and Tsien … WebOct 1, 1997 · Prasher, D., Eckenrode, V., Ward, W., Prendergast, R. and Cormier, M. 1992. Primary structure of the Aequorea victoriagreen-fluorescent protein.Gene 111: 229–233 ... WebJan 1, 2001 · The cloning of the green fluorescent protein (GFP) from the jellyfish Aequoria victoria and its expression in heterologous systems was a significant advance for optical microscopy of living cells ( Chalfie et al., 1994 ). imprimerie fontenay sous bois