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Venus荧光蛋白的激发光波长和发射光波长是多少

作者:激发光源事业部时间:2019-10-13 18:31:28浏览14779 次

信息摘要:

Venus荧光蛋白的激发光波长是515nm,发射光波长是529nm左右。Venus荧光蛋白属于黄色荧光蛋白的一种,所以,Venus荧光蛋白的发射光光谱图可参考黄色荧光蛋白的光谱图。Venus Fluorescence Protein is a basic (constitutively fluorescent) yellow fluorescent protein published in 2002, derived from Aequorea victoria. It is reported to be a rapidly-maturing weak dimer with moderate acid sensitivity.

Venus荧光蛋白的激发光波长是515nm,发射光波长是529nm左右。Venus荧光蛋白属于黄色荧光蛋白的一种,所以,Venus荧光蛋白的发射光光谱图可参考黄色荧光蛋白的光谱图。

Venus黄色荧光蛋白的激发光波长

Venus Fluorescence Protein

Venus is a basic (constitutively fluorescent) yellow fluorescent protein published in 2002, derived from Aequorea victoria. It is reported to be a rapidly-maturing weak dimer with moderate acid sensitivity.


Yellow  Fluorescence Proteins

Protein  Excitation (nm) Emission(nm) Notes
EYFP 513 527
Citrine 516 529 EYFP derivative; Less Cl, pH sensitive
Venus 515 528 EYFP derivative; 30-fold brighter at 37° C
SYFP2 515 527 improved Venus
TagYFP 508 524

如果要观察Venus黄色荧光蛋白(Venus Fluorescent Protein)的表达,美国路阳生产的便携式荧光蛋白激发光源可以选择LUYOR-3260CY和LUYOR-3415C(X)系列双波长荧光蛋白激发光源。黄色荧光蛋白采用青色光源激发,佩戴LUV-40A桔色观察眼镜观察,能够分选愈伤组织、菌落、植株、种子等黄色荧光蛋白表达阳性的目标,是转基因筛选的良好工具。如希望提供更多详细信息,可直接联系上海路阳生物技术有限公司的销售客服

下图为用于观察黄色荧光蛋白的便携式激发光源LUYOR-3415:

用于观察黄色荧光蛋白的便携式激发光源LUYOR-3415

下图为用于观察黄色荧光蛋白的观察眼镜LUV-40A:

用于观察黄色荧光蛋白的观察眼镜

下图为用于拍摄黄色荧光蛋白的拍照滤镜LUV-550A:

用于拍摄黄色荧光蛋白的拍照滤镜


Yellow Fluorescent Proteins

Yellow fluorescent protein (YFP) is a mutant variant of GFP. In this case, a mutation was introduced after the discovery that threonine residue was present near the chromophore in GFP.

To bring stability to the excited dipole moment of chromophore, this threonine residue was mutated. This led to shift by 20 nm in the excitation and emission wavelength of the fluorescent protein, leading to longer wavelengths.

YFP was further improved that led to development of enhanced yellow fluorescent protein or eYFP. This is one of the brightest fluorescent proteins and is widely used for different imaging purposes. GFP and YFP are used in several cases to perform dual imaging, which is a procedure where two molecules are tagged to two different fluorescent proteins. Consequently, they can be imaged together in order to visualize and appraise their inter-dynamics.

 


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