Experimental results of a satellite map of urban scene.

<p>Experimental results of a satellite map of urban scene.</p

Experimental results of the resolution test panel without alignment correction.

<p>Experimental results of the resolution test panel without alignment correction.</p

Phase distribution of original distorted wavefront of the resolution test panel experiment.

<p>Phase distribution of original distorted wavefront of the resolution test panel experiment.</p

Construction of primary mirror and dimension of segmented sub-aperture.

<p>Construction of primary mirror and dimension of segmented sub-aperture.</p

A set of random co-phase errors for simulation.

<p>A set of random co-phase errors for simulation.</p

Additional file 2: Figure S2. of Caveolin-1 regulates the expression of tight junction proteins during hyperoxia-induced pulmonary epithelial barrier breakdown

Effects of transfection concentration and transfection time of Cav-1 cDNA on mRNA and protein expression of Cav-1 in alveolar cell monolayers. At 48 h after transfection of 1 μg/mL Cav-1 cDNA, significant increases in caveolin-1 mRNA (A, B, E, F) and protein (C, D, G, H) were readily apparent. mRNA and protein expressions were determined by RT-PCR and Western blot analysis, respectively. β-actin was used as an internal control. Values are represented as means ± SD, ## P < 0.01 for comparison between the normoxia and CAV1 cDNA-transfected group, ** P < 0.01 for comparison between different concentration transfected groups or different time ransfected groups. (TIF 1801 kb

Experimental results of the resolution test panel with alignment correction.

<p>Experimental results of the resolution test panel with alignment correction.</p

Additional file 3: Figure S3. of Caveolin-1 regulates the expression of tight junction proteins during hyperoxia-induced pulmonary epithelial barrier breakdown

Efficacy assessment of Cav-1-siRNA transfection and pCMV6-CAV1 transfection. At 60–70 % confluence, cells exposed to normoxia were transfected with 10 nm of a control siRNA (Fluorescein Conjugate) (Cat.#6201;Cell Signaling Danvers MA) for 72 h to assess transfection efficiency for Cav-1-siRNA, while cells exposed to normoxia or hyperoxia were transfected with 1 μg/mL of pCMV6-AC-GFP (Cat.#PS100010; OriGene Technologies) for 48 h to assess transfection efficiency for pCMV6-CAV1. Images were obtained using a confocal laser scanning microscope at 100× magnification. Green represents transfected cells. The areas of transfected cells and all the cells in the view were measured by image pro plus software, and the ratio represents transfection efficiency. The transfection efficiency of control siRNA was (88.29 ± 8.25)% (A, B). The transfection efficiency of pCMV6-AC-GFP under normoxic conditions was (92.81 ± 4.16)% (C, D). The transfection efficiency of pCMV6-AC-GFP under hyperoxic conditions was (90.42 ± 6.83)% (E, F). (TIF 10078 kb

Experimental results of an actual image of the lunar eclipse.

<p>Experimental results of an actual image of the lunar eclipse.</p

Evaluation results of the wavefront detection accuracy and image restoration quality.

<p>Evaluation results of the wavefront detection accuracy and image restoration quality.</p