Misty Morning, in the Springtime...

I'm Brandon, I go to the University of Florida, and I like flowers, paintings, and paintings of flowers. And books.

šŸŒ»Insta/snap: brandoncorderšŸŒ¹

Misty Morning, in the Springtime...
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thisishowtheworldends:

Four Horsemen of the Apocalypse (1887) by Viktor Vasnetsov
Album Art
253 plays 
Album Art
587 plays 
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Céline F/W 2011
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whore-for-couture:

Haute Couture blog :)
Album Art
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Album Art
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freshphotons:

A 3D model of synaptic architecture. ”We used an integrative approach, combining quantitative immunoblotting and mass spectrometry to determine protein numbers; electron microscopy to measure organelle numbers, sizes, and positions; and super-resolution fluorescence microscopy to localize the proteins. Using these data, we generated a three-dimensional model of an “average” synapse, displaying 300,000 proteins in atomic detail.” Via.

I remember learning about some of those proteins. The general attitude was “those look NOTHING like what they look like in the textbook!!”
freshphotons:

A 3D model of synaptic architecture. ”We used an integrative approach, combining quantitative immunoblotting and mass spectrometry to determine protein numbers; electron microscopy to measure organelle numbers, sizes, and positions; and super-resolution fluorescence microscopy to localize the proteins. Using these data, we generated a three-dimensional model of an “average” synapse, displaying 300,000 proteins in atomic detail.” Via.

I remember learning about some of those proteins. The general attitude was “those look NOTHING like what they look like in the textbook!!”
freshphotons:

A 3D model of synaptic architecture. ”We used an integrative approach, combining quantitative immunoblotting and mass spectrometry to determine protein numbers; electron microscopy to measure organelle numbers, sizes, and positions; and super-resolution fluorescence microscopy to localize the proteins. Using these data, we generated a three-dimensional model of an “average” synapse, displaying 300,000 proteins in atomic detail.” Via.

I remember learning about some of those proteins. The general attitude was “those look NOTHING like what they look like in the textbook!!”
freshphotons:

A 3D model of synaptic architecture. ”We used an integrative approach, combining quantitative immunoblotting and mass spectrometry to determine protein numbers; electron microscopy to measure organelle numbers, sizes, and positions; and super-resolution fluorescence microscopy to localize the proteins. Using these data, we generated a three-dimensional model of an “average” synapse, displaying 300,000 proteins in atomic detail.” Via.

I remember learning about some of those proteins. The general attitude was “those look NOTHING like what they look like in the textbook!!”
freshphotons:

A 3D model of synaptic architecture. ”We used an integrative approach, combining quantitative immunoblotting and mass spectrometry to determine protein numbers; electron microscopy to measure organelle numbers, sizes, and positions; and super-resolution fluorescence microscopy to localize the proteins. Using these data, we generated a three-dimensional model of an “average” synapse, displaying 300,000 proteins in atomic detail.” Via.

I remember learning about some of those proteins. The general attitude was “those look NOTHING like what they look like in the textbook!!”
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Annie Clark photographed by Beth Herzhaft
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