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. 2009 Nov 20;10(10):4352–4374. doi: 10.3390/ijms10104352

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© 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland.

This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).

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Figure 8. — Immunofluorescence staining of talin, an integrin-associated protein of focal adhesion plaques, in rat aortic smooth muscle cells on day 5 after seeding on pristine PE (A), a reference material represented by a microscopic glass coverslip (B), PE irradiated with plasma (C), PE irradiated with plasma and grafted with glycine (D), polyethyleneglycol (E) bovine serum albumin (F), colloidal carbon particles (G) or bovine serum albumin and C (H).

Leica confocal laser scanning microscope (TCS SP2, Germany), obj. 100x, bar = 30 μm.

Figure 8. — Immunofluorescence staining of talin, an integrin-associated protein of focal adhesion plaques, in rat aortic smooth muscle cells on day 5 after seeding on pristine PE (A), a reference material represented by a microscopic glass coverslip (B), PE irradiated with plasma (C), PE irradiated with plasma and grafted with glycine (D), polyethyleneglycol (E) bovine serum albumin (F), colloidal carbon particles (G) or bovine serum albumin and C (H).

Leica confocal laser scanning microscope (TCS SP2, Germany), obj. 100x, bar = 30 μm.