a.k.a. SEYFP-F46L
similar: mVenus
Oligomerization | Organism | Molecular Weight | Cofactor |
---|---|---|---|
Weak dimer | Aequorea victoria | 26.8 kDa | - |
Ex λ | Em λ | EC (M-1 cm-1) | QY | Brightness | pKa | Maturation (min) | Lifetime (ns) |
---|---|---|---|---|---|---|---|
515 | 528 | 92,200 | 0.57 | 52.55 | 6.0 | 17.6 | 3.0 |
% Normal Cells | OSER/NE ratio | Cell Type | Reference |
---|---|---|---|
36.5 ± 3.5 (10000 cells) | - | HeLa | Cranfill et al. (2016) |
t1/2 (s) | Power | Light | Mode | In Cell | Fusion | ˚C | Reference |
---|---|---|---|---|---|---|---|
15.0 | Kremers et al. (2006) |
Venus was derived from SEYFP with the following mutations: F46L
amino acid numbers relative to avGFP. show relative to SEYFP
F46L accelerates the oxidation step, leading to the enhancement of fluorescence development of YFP at 37°C. The SEYFP-F46L variant folds and forms the chromophore very efficiently at 37°C.
Nagai et al. (2002)
(2002). Nature Biotechnology, 20(1) , 87-90. doi: 10.1038/nbt0102-87. Article Pubmed
(2017). Nature Methods, 15(1) , 47-51. doi: 10.1038/nmeth.4509. Article Pubmed
(2006). Biochemistry, 45(21) , 6570-6580. doi: 10.1021/bi0516273. Article Pubmed
(2002). Journal of Biological Chemistry, 277(52) , 50573-50578. doi: 10.1074/jbc.m209524200. Article Pubmed
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