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納米圖案灌流培養(yǎng)皿*,該細胞組織可拉伸微電極陣列刺激與成像記錄系統(tǒng)使研究人員能夠可重復(fù)且可靠地研究生理和病理機械拉伸對生物組織電生理的影響。該系統(tǒng)集成:細胞拉伸設(shè)備,電生理數(shù)據(jù)采集系統(tǒng);活細胞成像系統(tǒng)三種功能...

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納米圖案灌流培養(yǎng)皿*

納米圖案灌流培養(yǎng)皿,

品牌:法國 以及美國flexcell

銷售歐美進口各種不同基底靜態(tài)培養(yǎng)及不同基底力學(xué)刺激環(huán)境動態(tài)培養(yǎng)裝置
一、法國基底剛度可調(diào)控微圖案培養(yǎng)產(chǎn)品

特點:

控制細胞的3D結(jié)構(gòu)和力學(xué)

細胞在平坦或微結(jié)構(gòu)化的軟3D環(huán)境中培養(yǎng),以模仿體內(nèi)條件。

基材的剛度可以從非常軟(1 kPa)到非常硬(200 kPa)中選擇

提供多種基材形貌(平坦,圓形孔,方形孔,凹槽等)

基于凝膠的底物已準(zhǔn)備好用于您的細胞培養(yǎng)實驗

由于細胞直接接種在特征的頂部(易于限制非遷移細胞),因此易于使用且易于使用

預(yù)涂ECM基質(zhì)(例如纖連蛋白)

適用于任何細胞培養(yǎng)底物(蓋玻片,培養(yǎng)皿,多孔板)

凝膠的光學(xué)透明性使這些底物與高分辨率光學(xué)顯微鏡系統(tǒng)兼容

可拉伸細胞基底硬度控制培養(yǎng)皿(CellSoft 100mm Round Dishes)

Cells sense soft! CellSoft offers softer substrates to match the material properties of tissue niches to better meet the needs of biological laboratories wanting to grow their cells on native stiffness。

直徑100mm培養(yǎng)皿,總生長表面積為57cm2

BioFlex® CellSoft標(biāo)準(zhǔn)6孔板

腔室載玻片CellSoft

CellSoft培養(yǎng)板有很多不同的種類,如不同的硬度,不同的孔板,用于顯微觀察的腔室載玻片(圓形多孔板),共價包被CollagenI或其他蛋白,可對細胞進行靜態(tài)或動態(tài)牽拉應(yīng)力刺激。更重要的一點,新型的CellSoft培養(yǎng)板可以反復(fù)消化和再接種細胞,蛋白包被的表面可以重復(fù)使用多達三次。

niche。彈性模量范圍1-80kPa

BioFlex® CellSoft標(biāo)準(zhǔn)6孔板

腔室載玻片CellSoft

Amino,

Elastin,

and Laminin (YIGSR)
and untreated (未處理)

納米圖案化牽張、壓縮培養(yǎng)表面提供細胞微環(huán)境,模仿天然細胞外基質(zhì)的對齊結(jié)構(gòu),促進細胞結(jié)構(gòu)和功能發(fā)展。

    納米圖案化牽張、壓縮培養(yǎng)表面提供細胞微環(huán)境,模仿天然細胞外基質(zhì)的對齊結(jié)構(gòu),促進細胞結(jié)構(gòu)和功能發(fā)展。

    • PUBLICATIONS








      • Confinement and Low Adhesion Induce Fast Amoeboid Migration of Slow Mesenchymal Cells
        Y.-J. Liu, M. Piel, Cell, et al., 2015 160(4), 659-672


      • Actin flows induce a universal coupling between cell speed and cell persistence
        P. Maiuri, R. Voituriez, et al., Cell, 2015 161(2), 374–386


      • Geometric friction directs cell migration
        M. Le Berre, M. Piel, et al., Physical Review Letter 2013 111, 198101


      • Mitotic rounding alters cell geometry to ensure efficient spindle assembly
        O. M. Lancaster, B. Baum, et al., Developmental Cell, 2013 25(3), 270-283


      • Fine Control of Nuclear Confinement Identifies a Threshold Deformation leading to Lamina Rupture and Induction of Specific Genes
        M. Le Berre, J. Aubertin, M. Piel, Integrative Biology, 2012 4 (11), 1406-1414


      • Exploring the Function of Cell Shape and Size during Mitosis
        C. Cadart, H. K. Matthews, et al., Developmental Cell, 2014 29(2), 159-169


      • Methods for Two-Dimensional Cell Confinement
        M. Le Berre, M. Piel, et al., 2014, Micropatterning in Cell Biology Part C, Methods in cell biology, 121, 213-29



    • References



    • [1] D. Huh, G.A. Hamilton, and D. E. Ingber, “From 3D cell culture to organs-on-chips," TrendsCell Biol., vol. 21, no. 12, pp. 745–754, 2011.


    • [2] M. Ravi, V.Paramesh, S. R. Kaviya, E. Anuradha, and F. D. Paul Solomon, “3D cell culturesystems: Advantages and applications," J. Cell. Physiol., vol. 230,no. 1, pp. 16–26, 2015.


    • [3] J. W.Haycock, 3D cell culture: a review of current approaches andtechniques., vol. 695. 2011.


    • [4] F.Pampaloni, E. G. Reynaud, and E. H. K. Stelzer, “The third dimension bridgesthe gap between cell culture and live tissue.," Nat. Rev. Mol. CellBiol., vol. 8, no. 10, pp. 839–845, 2007.


    • [5] J. Lee, M.J. Cuddihy, and N. A. Kotov, “Three-dimensional cell culture matrices: state ofthe art.," Tissue Eng Part B Rev, vol. 14, no. 1, pp. 61–86, 2008.


    • [6] M.Vinci et al., “Advances in establishment and analysis ofthree-dimensional tumor spheroid-based functional assays for target validationand drug evaluation," BMC Biol., vol. 10, no. 1, p. 29, 2012.


    • [7] B. A.Justice, N. A. Badr, and R. A. Felder, “3D cell culture opens new dimensions incell-based assays," Drug Discov. Today, vol. 14, no. 1–2, pp.102–107, 2009.


    • [8] I.Meyvantsson and D. J. Beebe, “Cell culture models in microfluidicsystems.," Annu. Rev. Anal. Chem., vol. 1, pp. 423–449, 2008.


    • [9] E. W. K.Young and D. J. Beebe, “Fundamentals of microfluidic cell culture in controlledmicroenvironments," Chem Soc Rev, vol. 39, no. 3, pp. 1036–1048,2010.


    • [10] D. J.Beebe, G. a Mensing, and G. M. Walker, “Physics and applications ofmicrofluidics in biology.," Annu. Rev. Biomed. Eng., vol. 4, pp.261–286, 2002.


    • [11] J. El-Ali,P. K. Sorger, and K. F. Jensen, “Cells on chips.," Nature, vol.442, no. 7101, pp. 403–411, 2006.


    • [12] J.Guck et al., “Optical deformability as an inherent cell marker fortesting malignant transformation and metastatic competence," Biophys J,vol. 88, no. 5, pp. 3689–3698, 2005.


    • [13] S.Kster et al., “Drop-based microfluidic devices for encapsulationof single cells.," Lab Chip, vol. 8, no. 7, pp. 1110–1115, 2008.


    • [14] H.Andersson and A. Van den Berg, “Microfluidic devices for cellomics: Areview," Sensors Actuators, B Chem., vol. 92, no. 3, pp. 315–325,2003.


    • [15] M. W.Tibbitt and K. S. Anseth, “Hydrogels as extracellular matrix mimics for 3D cellculture," Biotechnol. Bioeng., vol. 103, no. 4, pp. 655–663, 2009.


    • [16] J. P.Vacanti and R. Langer, “Tissue engineering: the design and fabrication ofliving replacement devices for surgical reconstruction andtransplantation.," Lancet, vol. 354, p. SI32-I34, 1999.


    • [17] G. S. D.Hetal Patel, Minal Bonde, “Biodegradable polymer scaffolds for tissueengineering," Trends Biomater. Artif. Organs, vol. 25, no. 1, pp.20–29, 2011.


    • [18] L. G.Griffith and M. A. Swartz, “Capturing complex 3D tissue physiology invitro.," Nat. Rev. Mol. cell Biol., vol. 7, no. 3, pp. 211–24,2006.


    • [19] D. J.Tobin, “Scaffolds for Tissue Engineering and 3D Cell Culture," MethodsMol. Biol., vol. 695, no. 2, pp. 213–227, 2011.


    • [20] J.Naranda et al., “Polyester type polyHIPE scaffolds with an interconnectedporous structure for cartilage regeneration," Sci. Rep., vol. 6,no. February, p. 28695, 2016.


    • [21] B.Dhandayuthapani, Y. Yoshida, T. Maekawa, and D. S. Kumar, “Polymeric scaffoldsin tissue engineering application: A review," Int. J. Polym. Sci.,vol. 2011, no. ii, 2011.


    • [22] F. J.O’Brien, “Biomaterials & scaffolds for tissue engineering," Mater.Today, vol. 14, no. 3, pp. 88–95, 2011.


    • [23] A. L.Paguirigan and D. J. Beebe, “Microfluidics meet cell biology: Bridging the gap byvalidation and application of microscale techniques for cell biologicalassays," BioEssays, vol. 30, no. 9, pp. 811–821, Sep. 2008.


    • [24] F.-Q. Nie,M. Yamada, J. Kobayashi, M. Yamato, A. Kikuchi, and T. Okano, “On-chip cellmigration assay using microfluidic channels.," Biomaterials, vol.28, no. 27, pp. 4017–4022, 2007.


    • [25] A. Valster,N. L. Tran, M. Nakada, M. E. Berens, A. Y. Chan, and M. Symons, “Cell migrationand invasion assays," Methods, vol. 37, no. 2, pp. 208–215, 2005.


    • [26] C. R.Justus, N. Leffler, M. Ruiz-Echevarria, and L. V Yang, “In vitro cell migrationand invasion assays.," J. Vis. Exp., vol. 752, no. 88, p. e51046,2014.


    • [27] N.Kramer et al., “In vitro cell migration and invasionassays.," Mutat Res, vol. 752, no. 1, pp. 10–24, 2013.


    • [28] J. W. Hong,V. Studer, G. Hang, W. F. Anderson, and S. R. Quake, “A nanoliter-scale nucleicacid processor with parallel architecture.," Nat. Biotechnol., vol.22, no. 4, pp. 435–439, 2004.


    • [29] J. Q.Boedicker, L. Li, T. R. Kline, and R. F. Ismagilov, “Detecting bacteria anddetermining their susceptibility to antibiotics by stochastic confinement innanoliter droplets using plug-based microfluidics.," Lab Chip, vol.8, no. 8, pp. 1265–1272, 2008.


    • [30] G.Velve-Casquillas, M. Le Berre, M. Piel, and P. T. Tran, “Microfluidic tools forcell biological research," Nano Today, vol. 5, no. 1. pp. 28–47,2010.


    • [31] C. R.Terenna et al., “Physical Mechanisms Redirecting Cell Polarity andCell Shape in Fission Yeast," Curr. Biol., vol. 18, no. 22, pp.1748–1753, . 2008.


    • [32] G.Faure-andré, “Regulation of Dendritic Cell Migration by CD74, the MHC ClassII–Associated Invariant Chain," Science (80-. )., vol. 1705, no.December, 2008.


    • [33] S. M.McFaul, B. K. Lin, and H. Ma, “Cell separation based on size and deformabilityusing microfluidic funnel ratchets," Lab Chip, vol. 12, no. 13, pp.2369–2376, 2012.


    • [34] S. C. Hur,N. K. Henderson-MacLennan, E. R. B. McCabe, and D. Di Carlo,“Deformability-based cell classification and enrichment using inertialmicrofluidics.," Lab Chip, vol. 11, no. 5, pp. 912–920, 2011.


    • [35] H. W. Hou,Q. S. Li, G. Y. H. Lee, A. P. Kumar, C. N. Ong, and C. T. Lim, “Deformabilitystudy of breast cancer cells using microfluidics," Biomed. Microdevices,vol. 11, no. 3, pp. 557–564, 2009.




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