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Scanning electron microscopy images of platelets stimulated by collagen in the presence of licochalcones.

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posted on 2017-03-10, 18:44 authored by Asa Okuda-Tanino, Daiki Sugawara, Takumi Tashiro, Masaya Iwashita, Yutaro Obara, Takahiro Moriya, Chisato Tsushima, Daisuke Saigusa, Yoshihisa Tomioka, Kuniaki Ishii, Norimichi Nakahata

Platelets were incubated with collagen (3 μg/ml) for 3 min in the presence or absence of licochalcones (100 μM), then fixed overnight with 1% glutaraldehyde. The samples were washed twice for 5 min with PBS. The fixed platelets were dehydrated with ethanol and t-butyl alcohol, and after the samples were freeze-dried and coated with Au/Pd, they were observed under a scanning electron microscope. (A) Unstimulated platelets, (B) collagen (3 μg/ml), (C) licochalcone A (100 μM) +collagen, (D) licochalcone C (100 μM) +collagen and (E) licochalcone D (100 μM) +collagen. (Magnification: 7000×, bar = 5 μm).

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