<p>(A) The cell line L929 was cultured on a positive control substrate (Ctrl), on gelatin gel (g gel) and on quattroGel (qGel), metabolically marked with bromodeoxyuridine (BrdU, green) to identify mitotic cells and cytochemically labeled with fluorescent phalloidin (actin, red) and DAPI (blue) to display all cell nuclei. Pictures of individual rows represent corresponding images. Arrows mark cells in different stages of mitosis. Quantification of cell adhesion (B) and cell proliferation (C) indicate that no statistically significant differences exist between different substrates. n = 3, s.d., p<0.05. Scale bar: (A) 50 µm.</p
<p>(A) Phase contrast photomicrographs showing primary cultures of BM-MSCs (day 7) from Mutant, Lean...
<p>C2C12 cells cultured and differentiated on PDMS (A) 1.72MPa, (B) 830 kPa, (C) 130 kPa, (D) 50 kPa...
<p>Cells were allowed to attach for 6 hours, followed by fixation and staining with Alexa Fluor 594 ...
<p>(A-C) Human umbilical vascular endothelial cells (HUVEC) were cultured on a positive control subs...
<p>(A) HeLa cells (YFP-paxillin) were cultured on 2D square patterns for 18 hours and imaged during ...
<p>(A) The substrate compliance was measured in 0.5 cm increments using spherical indentation testin...
<p>(A,B) Integration and establishment of BM-MSCs on Gelfoam after 3 days of culturing. <i>A</i>, lo...
<p>(A) Plating efficiency calculated as a ratio of MSCs adherent to scaffolds following a 48-hour in...
<p>HeLa cells (RFP-tubulin/GFP-H2B) were synchronized and cultured on 2D homogenously coated substra...
<p>(A-C) Human chondrocytes were cultured on a positive control substrate (Ctrl), on gelatin gel (g ...
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
<p>On dynamic substrates fibroblasts were patterned on various sizes of circles and lines. Cells pro...
<p>(A) Schematic representation of experimental setup used to quantify cell association of fluoresce...
<p>(a) Representative phase contrast images of NIH 3T3 fibroblasts cultured on 1.5, 2.5 and 40 kPa p...
<p>MSC were seeded in equal numbers (1000 cells/cm<sup>2</sup>) on tissue culture dishes which were ...
<p>(A) Phase contrast photomicrographs showing primary cultures of BM-MSCs (day 7) from Mutant, Lean...
<p>C2C12 cells cultured and differentiated on PDMS (A) 1.72MPa, (B) 830 kPa, (C) 130 kPa, (D) 50 kPa...
<p>Cells were allowed to attach for 6 hours, followed by fixation and staining with Alexa Fluor 594 ...
<p>(A-C) Human umbilical vascular endothelial cells (HUVEC) were cultured on a positive control subs...
<p>(A) HeLa cells (YFP-paxillin) were cultured on 2D square patterns for 18 hours and imaged during ...
<p>(A) The substrate compliance was measured in 0.5 cm increments using spherical indentation testin...
<p>(A,B) Integration and establishment of BM-MSCs on Gelfoam after 3 days of culturing. <i>A</i>, lo...
<p>(A) Plating efficiency calculated as a ratio of MSCs adherent to scaffolds following a 48-hour in...
<p>HeLa cells (RFP-tubulin/GFP-H2B) were synchronized and cultured on 2D homogenously coated substra...
<p>(A-C) Human chondrocytes were cultured on a positive control substrate (Ctrl), on gelatin gel (g ...
<p>(a) Colorimetric viability test showed that cells flowed through the device remain highly viable ...
<p>On dynamic substrates fibroblasts were patterned on various sizes of circles and lines. Cells pro...
<p>(A) Schematic representation of experimental setup used to quantify cell association of fluoresce...
<p>(a) Representative phase contrast images of NIH 3T3 fibroblasts cultured on 1.5, 2.5 and 40 kPa p...
<p>MSC were seeded in equal numbers (1000 cells/cm<sup>2</sup>) on tissue culture dishes which were ...
<p>(A) Phase contrast photomicrographs showing primary cultures of BM-MSCs (day 7) from Mutant, Lean...
<p>C2C12 cells cultured and differentiated on PDMS (A) 1.72MPa, (B) 830 kPa, (C) 130 kPa, (D) 50 kPa...
<p>Cells were allowed to attach for 6 hours, followed by fixation and staining with Alexa Fluor 594 ...