Product Description
ThisCytoSoft®Imaging96-well product has a defined elastic modulus (see certificate of analysis) with a glass bottom for high resolution imaging The thickness of the silicone gel is uniform with a ~0.03 mm thick layer of silicone in each well.The silicone gels are activated and ready to bind to a purified ECM, such as PureCol® type I collagen (#5005) prior to cell addition.
The rigidity of the substrate to which cells adhere can have a profound effect on cell morphology and gene expression.CytoSoft®products provide a tool to culture cells on substrates with various rigidities covering a broad physiological range using a thin layer of biocompatible silicone.
TheCytoSoft®–Imagingplate has a glass bottom for high-resolution imaging where low autofluorescence and exceptional optical clarity are required. The 96-well format is optimal for high-throughput cell studies and screening. The plate consists of a #1.5 thickness glass bottom bonded to a black polystyrene frame and includes a lid. The plates are sterilized using ozone and provided with 1 plate per package.
On the bottom of each well, there is a thin layer of specially formulated biocompatible silicone, whose elastic modulus (rigidity) is carefully measured and certified. The surfaces of the gels inCytoSoft®products are functionalized to form covalent bonds with amines on proteins. The chemical functionalization is stable and the reaction does not require a catalyst, facilitating coating of the gel surfaces with matrix proteins and plating cells.
The silicone substrates are optically clear and have a near zero auto-florescence. The layer of silicone in each well is firmly bonded to the bottom of the well. Unlike hydrogels (such as polyacrylamide gels), silicone gels are not susceptible to hydrolysis, do not dry or swell, are resilient and resistant to tearing or cracking, and their elastic moduli (rigidities) remain nearly unchanged during extended storage times.
CytoSoft®-Imagingproducts accommodate live cell staining using membrane and cell permeable dyes; fixation of cells using common techniques such as paraformaldexyde; and immunostaining of fixed cells.
| Parameter, Testing, and Method | CytoSoft®Imaging 96-Well Plates |
| Sterilization Method | Ozone |
| Plate Size | 96-Multiwell Black Polystyrene Plate with Glass Bottom |
| Quantity per Package | 1 Plate |
| Rigidty (Elastic Modulus) | 0.2, 0.5, 2, 8, 16, 32, 64 kPa (exact values provided on the CofA) |
| Storage Temperature | Room Temperature |
| Shelf Life | Minimum of 6 months from date of receipt |
| Plate Surface Material | Functionalized Silicone |
Growth Area per Well | 0.32cm2 |
Typical Working Volume per Well | 40 to 280 μL |
Cell Attachment Assay | Pass |
Directions for Use
Download the full PDF versionor continue reading below:
Coating Procedure
Note:Use these recommendations as guidelines to determine the optimal coating conditions for your culture system.
Cautionary Note: The bottom of a 96-well plate can be detached by excessive mechanical force such as centrifugation or direct contact with liquid handling tools (tips, pipettes, etc.).
Remove theCytoSoft®product from the protective sleeve in a sterile hood.
- Prepare extracellular matrix material by neutralizing in amine-free buffer pH 7.4 to 7.9 (such as 1X DPBS). We do not recommend using gelatin as your ECM protein.
Note: Pre-warm the coating solution to approximately room temperature before use.
- Dilute as needed, and dispense ~150 uL of solution into each well to fully coat the surface.
Note:Recommended dilution for PureCol®3 mg/ml Type I collagen is 1:30 (~100 µg/ml).
Note: The hydrophobic surface requires larger volumes to cover the surface than do conventional plastic dishes
- Incubate ECM coatedCytoSoft®at room temperature, covered for 0.5-1 hour.
- After incubation, aspirate any remaining material and rinse coated surfaces immediately two times with culture medium or PBS. Leave about 150 uL of medium per well to keep surface covered.
Note: Do not allow theCytoSoft® surface to become dry once the surface has been wetted.
- Coated surfaces are ready for use.
- Standard harvesting procedures used for removing cells from cultureware can be employed for harvesting cells from the CytoSoft® product including use of trypsin, Accutase® and non-enzymatic cell detachment solutions.
Product Q & A
We recommend a 60X objective for the imaging plates.
The elastic modulus is measured by tracking beads on the gel surface under a wide-field fluorescence microscope without any other specialized equipment. The measurements have small and simple to estimate errors and their results are confirmed by conventional tensile tests. A master curve is obtained relating the mixing ratios of the two components of Sylgard 184 with the resulting elastic moduli of the gels.
Using prewarmed media will decrease gas solubility and help prevent bubbles on the surface of the silicone.
The silicone gel can crack if the surface becomes dry.
No. Cell matrix proteins are attached to the surface of the gel via covalent bonding. It is difficult to form a new ECM layer after cell detachment. There are no longer any reactive groups on the surface of the gel after the initial cell culture.
The change in the refractive index of the silicone distorts things a little, so DIC will be possible but not perfect. Also, DIC is only possible on the glass bottom imaging plates, not the 6-well plastic plates.
1.41
The two main issues are:
1. Ineffecient coating of the matrix proteins due to low pH of the coating solution.
2. Insufficient wash of leftover cell matrix after the coating procedure.
No. Cytosoft must be coated with an ECM protein such as Collagen or Fibronectin.
The surface is decorated with anhydride functional groups.
Plasma use is not recommended. Plasma will induce formation of a hard crust on the surface and will change the mechanical properties of the CytoSoft® products.
Do not freeze the CytoSoft® products.
When frozen, there is a good chance that the silicone surface gets hydrolyzed and absorbs moisture, which would inactivate the binding sites and make the product not-usable.
If you froze the product and it is still frozen, warm the CytoSoft® up at 60C with the bag vented. That will minimize the chance of them absorbing moisture – but there is still a chance that they will no longer be functional.
Using gelatin for coating CytoSoft is often problematic because gelatin often has low molecular weight impurities that block binding sites on the activated surface of the silicone. We recommend using highly purified ECM's instead.
Product Cell Assay
CytoSoft®plates can also be used to show howfibroblastsare able to discriminate between the underlying stiffness. This ismanifested in both adhesion size andstress fibers, as seen below. It appears that the cells on the 8 kPa stiffness havereduced intracellular tension and increasedadhesion.
Product References
References for CytoSoft® Products:
1. Modaresi, Saman, et al. “Deciphering the Role of Substrate Stiffness in Enhancing the Internalization Efficiency of Plasmid DNA in Stem Cells Using Lipid-Based Nanocarriers.”Nanoscale, vol. 10, no. 19, 2018, pp. 8947–8952., doi:10.1039/c8nr01516c.
2. Wilson, Christina L.In Vitro Models Of Brain For Study Of Molecular Mechanisms In Brain Disorder. The University of Nebraska-Lincoln, 2016.
3. Wilson, C. L., Hayward, S. L., & Kidambi, S. (2016). Astrogliosis in a dish: Substrate stiffness induces astrogliosis in primary rat astrocytes.RSC Advances,6(41), 34447-34457. doi:10.1039/c5ra25916a
4. Prager-Khoutorsky M, Lichtenstein A, Krishnan R, Rajendran K, Mayo A, Kam Z, Geiger B, Bershadsky AD. Fibroblast polarization is a matrix-rigidity-dependent process controlled by focal adhesion mechanosensing. Nat. Cell Biol. 2011; 13:1457–1465.
5. Gutierrez E, Tkachenko E, Besser A, Sundd P, Ley K, Danuser G, Ginsberg MH, Groisman A. High Refractive Index Silicone Gels for Simultaneous Total Internal Reflection Fluorescence and Traction Force Microscopy of Adherent Cells. PLoS One. 2011; 6:e23807.
6. Merkel R, Kirchgessner N, Cesa CM, Hoffmann B. Cell force microscopy on elastic layers of finite thickness. Biophys. J. 2007; 93:3314–23.
7. Schellenberg, A. et al. Matrix elasticity, replicative senescence and DNA methylation patterns of mesenchymal stem cells. Biomaterials 35, 6351–8 (2014).
8. Cesa, C. M. et al. Micropatterned silicone elastomer substrates for high resolution analysis of cellular force patterns. Rev. Sci. Instrum. 78, 034301 (2007).
9. Gutierrez, E. & Groisman, A. Measurements of Elastic Moduli of Silicone Gel Substrate with a Micro fluidic Device. Plos One 6 (2011).
10. Mori, H., Takahashi, A., Horimoto, A., and Hara, M. Migration of glial cells differentiated from neurosphere-forming neural stem/progenitor cells depends on the stiffness of the chemically cross-linked collagen gel substrate. Neuroscience Letters, Vol. 555, October (2013)
11. Banerjee, I., Carrion, K., Serrano, R., Dyo, J., Sasik, R., Lund, S. et al.Cyclic stretch of embryonic cardiomyocytes increases proliferation, growth, and expression while repressing Tgf-β signaling.J Mol Cell Cardiol.2015;79:133–144
12. Vertelov, G.et al. Rigidity of silicone substrates controls cell spreading and stem cell differentiation.Sci. Rep.6, 33411; doi: 10.1038/srep33411 (2016).
13. Tkachenko E, Rawson R, La E, et al. Rigid Substrate Induces Esophageal Smooth Muscle Hypertrophy and EoE Fibrotic Gene Expression.The Journal of allergy and clinical immunology. 2016;137(4):1270-1272.e1. doi:10.1016/j.jaci.2015.09.020.
14. Sao, K.et al.Myosin II governs intracellular pressure and traction by distinct tropomyosin-dependent mechanisms.Molecular Biology of the Cell30,1170–1181 (2019).
15.Cooper, J. G.et al.Spinal Cord Injury Results in Chronic Mechanical Stiffening.Journal of Neurotrauma(2019). doi:10.1089/neu.2019.6540
Product Certificate of Analysis
Product Videos
What is CytoSoft®?
Video
How to Coat CytoSoft® Plates
Video
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Safety and Documentation
Safety Data Sheet
Certificate of Origin
Product Disclaimer
This product is for R&D use only and is not intended for human or other uses. Please consult the Material Safety Data Sheet for information regarding hazards and safe handling practices.
美国AdvancedBioMatrix（简称ABM） www.advancedbiomatrix.comAdvancedBioMatrix（简称ABM）是美国一家著名的生物公司，获得了AllerganInc的授权(Allergan用25年时间不断完善胶原蛋白相关的产品的生产工艺)，将Allergan的专业和技术用于蛋白生产与检测，致力于为组织工程、细胞分析及细胞增殖等研究领域提供优质稳定的产品。AdvancedBioMatrix不断丰富已有产品线，目前可为三维细胞培养提供各种胶原蛋白、纤连蛋白、玻连蛋白、水性凝胶、不同粘度与分子量的透明质酸以及低代成纤维细胞等。在美国全部产品授权Sigma销售。AdvancedBioMatrix是组织培养，细胞分析和细胞增殖三维（3D）应用的生命科学领域的领导者。我们的产品被公认为纯度，功能性和一致性的标准。我们在生产，分离，纯化，冷冻干燥，细胞培养和蛋白质测试，粘附肽，附着因子，底物刚性和其他3D矩阵产品方面拥有丰富的专业知识。我们的专业技术和知识正在被用来确保我们的产品质量最高，批次之间一致且易于为我们的研究客户使用。
美国AdvancedBioMatrix是3D组织培养、细胞检测和细胞增殖等领域实验解决方案的佼佼者。AdvancedBioMatrix在分离、纯化、冻干、细胞培养和蛋白检测、多肽粘附、附着因子、基质硬度和其他3Dmatrix 产品开发方面有着丰富的经验。AdvancedBioMatrix的研发经验和专业知识确保其产品可达到最佳质量，并保证产品之间一致性，方便研究客户使用。以下为AdvancedBioMatrix3DMatrices 产品竞争优势：1. 提供高纯度和成分确定的胞外基质；2. 超过1000余篇文献引用PureCol产品，品质非常均一；3. 在3D培养基领域可提供最全面的产品线；4. 唯一可提供特异性刚性有机硅基板的公司（CytoSoft）;5. 唯一可提供可溶性丝纤蛋白的供应商（可运用于多种3D培养）；6. 如果客户首次接触3D胶原凝胶，AdvancedBioMatrix还是唯一的预制胶原蛋白(PureColEZGel)供应商；
以下产品为AdvancedBioMatrix全球畅销品：1.PureCol 牛源I型胶原蛋白 3mg/ml#5005-100ML2.Nutragen牛源I型胶原蛋白 6mg/ml#5010-50ML3.FibriCol 牛源I型胶原蛋白 10mg/ml#5133-20ML4.VitroCol 人源I型胶原蛋白 #5007-20ML5. 弹性蛋白原 #5052-1MG6.ECMSelectArraykitUltra-36#5170-1EA7.CytoSoft（刚性可变的基底，AdvancedBioMatrix最新添加产品5190-7EA）8. 人III型胶原蛋白 #5021-10MG9. 人IV型胶原蛋白 #5022-5MG10.SilkFibroin溶液 #5154-20ML11.Fibronectin#5080-5MG12.Vitronectin#5051-0.1MG
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