The novel buffalo β-caesin promoter along with exon1, intron1 and exon2 is isolated and cloned upstream of the Enhanced Green flourescence protein (EGFP) gene and sequenced.
Preferably, the marker/reporter protein is a fluorescent protein, for example a green fluorescent protein, modified for enhanced fluorescence.
The non-oligomerizing fluorescent proteins can be derived from a naturally occuring green fluorescent protein, a red fluorescent protein, or other fluorescent protein, or a fluorescent protein related thereto.
The present invention provides fusion protein comprising IλB and green fluorescent protein.
The preferred fluorescent protein sensors are variants of the green fluorescent protein (GFP) from Aequora victoria.
Finally, this invention provides various uses of a green fluorescent protein.
A green fluorescent protein complex comprising a first green fluorescent protein, a primary ligand-binding peptide, and a second green fluorescent protein, is also disclosed.
Green fluorescent protein — EGFP redirects here.
Green fluorescence protein and Cu/Zn-superoxide dismutate (SOD) are used as the target protein.
In this case, the protein is green fluorescent protein.
The invention relates to a method for overproducing the green fluorescent protein (GFP).
The present invention provides mutants of the Green Fluorescent Protein (GFP) of Aequorea victoria.
The present invention also relates to microarrays having a tagged-green fluorescent protein.
In this regard, the green fluorescent protein (GFP) served as an indicator.
This protein is called the green fluorescent protein or GFP.
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