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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 9. — Immunofluorescence staining of contractile protein alpha-actin in rat aortic smooth muscle cells on day 5 after seeding on pristine PE (A), reference materials represented by a microscopic glass coverslip (B), a standard cell culture polystyrene dish (C), PE irradiated with plasma (D), PE irradiated with plasma and grafted with glycine (E), polyethyleneglycol (F), bovine serum albumin (G), colloidal carbon particles (H) or bovine serum albumin and C (I).

Olympus IX 51 microscope, DP 70 digital camera, obj. 100× (A, B, D-I) or 40× (C). Bar = 20 μm (A, B, D-I) or 100 μm (C).

Figure 9. — Immunofluorescence staining of contractile protein alpha-actin in rat aortic smooth muscle cells on day 5 after seeding on pristine PE (A), reference materials represented by a microscopic glass coverslip (B), a standard cell culture polystyrene dish (C), PE irradiated with plasma (D), PE irradiated with plasma and grafted with glycine (E), polyethyleneglycol (F), bovine serum albumin (G), colloidal carbon particles (H) or bovine serum albumin and C (I).

Olympus IX 51 microscope, DP 70 digital camera, obj. 100× (A, B, D-I) or 40× (C). Bar = 20 μm (A, B, D-I) or 100 μm (C).