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excellness彈性細胞培養板,excellness彈性細胞培養皿,excellness彈性細胞培養蓋玻片
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excellness彈性細胞培養板,excellness彈性細胞培養皿,excellness彈性細胞培養蓋玻片
備有現貨！
Simple, biomimetic tissue culture devices.
Think soft!
The physical properties of the substrate on which cells are grown profoundly influences the culture, as recent scientific data demonstrates. Substrate elasticity is as powerful to determine cell behavior and identity as is their chemical milieu.
Grow soft!
ExCellness provides non-degradable tissue culture surfaces with the elasticity of human tissue, ranging from the stiffness of bone to the softness of brain. Culturing your cells on our adapted culture substrates makes them "FEELING AT HOME"!
Enjoy soft!
Culturing your cells on ExCellness tailored culture substrates allows to:
- determine the optimal mechanical conditions for cells to express proteins of interest appropriay
- model healthy and diseased tissues in vitro
- determine the effect of substrate elasticity on cell proliferation rates, apoptosis, cytokine production, metabolism...
Our solution : biomimetic, elastic cell culture substrates
Our technology is based on the fact that the softness of the culture surface influences cell performance. We offer culture dishes with elastic surfaces that imitate the physical properties of tissues in the human body, ranging from the stiffness of bone to the softness of brain tissues.
PrimeCoat series
The ExCellness PrimeCoat series is designed specifically to provide a biomimetic cell culture environment that improves cell characteristics and phenotype in laboratory applications.
Key features
- PrimeCoat elastic substrates are easy to use for cell culture and subsequent analysis.
- PrimeCoat elastic substrates are available with 6 degrees of softness within the elasticity range of body tissues: 2, 5, 10, 15, 30 and 100 kPa.
- PrimeCoat elastic substrates are available in 4 standard formats: 100 mm diameter dishes, 40 mm diameter dishes, 24-well plates and 20x20 mm cover slips.
- PrimeCoat elastic substrates require to be coated by the end user to promote cell adhesion.
- PrimeCoat elastic substrates are transparent. Cells can be visualized with standard transmission light microscopes (e.g., Phase contrast, DIC).
- PrimeCoat elastic substrates are compatible with most standard molecular or cellular techniques: immunofluorescence, immunohistochemistry, protein analysis (e.g., Western blotting, and RNA/DNA extraction).
Biomimetic cell culture substrates at reach
PrimeCoat series combines simplicity and accessibility:
- simplicity of cell handling
- straightforward compatibility with cell analysis tools
- accessible prices
ExCellness in selected peer reviewed publications
In the following peer-reviewed publications, ExCellness biomimetic cell culture devices have been used or cited:
- N. Vedrenne et al. Isolation of astrocytes displaying myofibroblast properties and present in multiple sclerosis lesions. Neurochem. Res. 2017 Apr 22.
- X. L. Chen et al. MicroRNA-21 preserves the fibrotic mechanical memory of mesenchymal stem cells. Nature Materials 16, 379–389 (2017)
- M. R. Zeglinski et al. Chronic expression of Ski induces apoptosis and represses autophagy in cardiac myofibroblasts. Biochim. Biophys. Acta. 2016 Jun;1863(6 Pt A):1261-8
- H Chen et al. Mechanosensing by the α6-integrin confers an invasive fibroblast phenotype and mediates lung fibrosis. Nat. Commun. 2016 Aug 18;7: 12564.
- NP Talele et al. Expression of α-Smooth Muscle Actin Determines the Fate of Mesenchymal Stromal Cells. Stem Cell Reports. 2015 Jun 9;4(6) : 1016-30.
- V Sarrazy et al. Integrins avb5 and avb3 promote latent TGF-beta 1 activation by human cardiac fibroblast contraction. Cardiovasc Res (2014) 102 (3)
- VF Achterberg et al. The nano-scale mechanical properties of the extracellular matrix regulate dermal fibroblast function.J Invest Dermatol. 2014 Jul;134(7):1862-72.
- JA Cadby et al. Differences between the Cell Populations from the Peritenon and the Tendon Core with Regard to Their Potential Implication in Tendon Repair. 2014. PLoS ONE 9(3): e92474.
- T. Grand et al. Aggravation of Cardiac Myofibroblast Arrhythmogeneicity by Mechanical Stress. Cardiovasc Res. 2014 Dec 1;104(3):489-500.
- JA Cadby. Can we improve tendon healing in the horse? A multi-angle study of a multi-facet problem. ISBN: 978-90-5335-715-6
- A Vashist et al. Recent advances in hydrogel based drug delivery systems for the human body. J. Mater. Chem. B, 2014,2, 147-166
- EP van der Veer et al. The RNA-Binding Protein Quaking is a Critical Regulator of Vascular Smooth Muscle Cell Phenotype. Circ Res. 2013 Oct 12;113(9):1065-75.
- A De Boeck et al. Differential secretome analysis of cancer-associated fibrobroblasts and bone marrow-derived precursors toidentify microenvironmental regulators of colon cancerprogression. Proteomics 2013,13,379-388
- C Godbout et al. The Mechanical Environment Modulates Intracellular Calcium Oscillation Activities of Myofibroblasts.PLoS One. 2013; 8(5): e64560.
- S Constant et al. Colon Cancer: Current Treatments and Preclinical Models for the Discovery and Development of New Therapies. Drug discovery; Editor Hany A. El-Shemy. ISBN 978-953-51-0906-8.
- JL Balestrini et al. The mechanical memory of lung myofibroblasts. Integr. Biol., 2012,4, 410-421.
- Stem Cells and Cancer Stem Cells, Volume 8. Therapeutic Applications in Disease and Injury. Editors M.A. Hayat. ISBN 978-94-007-4797-5
- A Skardal et al. Bioprinted amniotic fluid-derived stem cells accelerate healing of large skin wounds. Stem Cells Transl Med. 2012 Nov;1(11):792-802. doi: 10.5966/sctm.2012-0088. Epub 2012 Oct 29.
- A Skardal et al. Substrate elasticity controls cell proliferation, surface marker expression and motile phenotype in amniotic fluid-derived stem cells. J Mech Behav Biomed Mater. 2013 January; 17: 307-316.
- BJ Crider et al. Myocardin-Related Transcription Factors A and B Are Key Regulators of TGF-b1-Induced Fibroblast to Myofibroblast Differentiation. Journal of Investigative Dermatology (2011) 131, 2378-2385
- L Follonier Casla et al. A new lock-step mechanism of matrix remodelling based on subcellular contractile events. Journal of Cell Science 123, 1751-1760
