نتایج جستجو برای: 2 dimensional cell culture

تعداد نتایج: 4287680  

Journal: :Biomaterials 2009
Kyung Eun Sung Gui Su Carolyn Pehlke Steven M Trier Kevin W Eliceiri Patricia J Keely Andreas Friedl David J Beebe

Interest in constructing a reliable 3-dimensional (3D) collagen culture platform in microfabricated systems is increasing as researchers strive to investigate reciprocal interaction between extracellular matrix (ECM) and cells under various conditions. However, in comparison to conventional 2-dimensional (2D) cell culture research, relatively little work has been reported about the polymerizati...

Journal: :iranian journal of immunology 0
neda mousavi niri department of immunology mansooreh jaberipour shiraz institute for cancer research, shiraz university of medical sciences, shiraz, iran mahboobeh razmkhah shiraz institute for cancer research, shiraz university of medical sciences, shiraz, iran abbas ghaderi department of immunology mojtaba habibagahi department of immunology

background: several studies have demonstrated the immunosuppresive effects of mes-enchymal stem cells (mscs) in allogeneic or mitogenic interactions. cell-cell contact inhibition and secretion of suppressive soluble factors have been suggested in this re-gard. objective: to investigate if adipose derived mscs could inhibit jurkat lym-phoblastic leukemia t cell proliferation during coculture. me...

Journal: :BioTechniques 2007
Anthony P Napolitano Dylan M Dean Alan J Man Jacquelyn Youssef Don N Ho Adam P Rago Matthew P Lech Jeffrey R Morgan

Techniques that allow cells to self-assemble into three-dimensional (3-D) spheroid microtissues provide powerful in vitro models that are becoming increasingly popular--especially in fields such as stem cell research, tissue engineering, and cancer biology. Unfortunately, caveats involving scale, expense, geometry, and practicality have hindered the widespread adoption of these techniques. We p...

2015
Cynthia A. Batchelder Michele L. Martinez Nadire Duru Frederick J. Meyers Alice F. Tarantal Feng Zhao

Renal cell carcinomas arise from the nephron but are heterogeneous in disease biology, clinical behavior, prognosis, and response to systemic therapy. Development of patient-specific in vitro models that efficiently and faithfully reproduce the in vivo phenotype may provide a means to develop personalized therapies for this diverse carcinoma. Studies to maintain and model tumor phenotypes in vi...

Journal: :Journal of visualized experiments : JoVE 2008
Eric Gottwald Brigitte Lahni David Thiele Stefan Giselbrecht Alexander Welle Karl-Friedrich Weibezahn

We have developed a chip-based cell culture system for the three-dimensional cultivation of cells. The chip is typically manufactured from non-biodegradable polymers, e.g., polycarbonate or polymethyl methacrylate by micro injection molding, micro hot embossing or micro thermo-forming. But, it can also be manufactured from bio-degradable polymers. Its overall dimensions are 0.7 1 x 20 x 20 x 0....

Journal: :Nature nanotechnology 2008
Y Shona Pek Andrew C A Wan Asha Shekaran Lang Zhuo Jackie Y Ying

Thixotropic materials, which become less viscous under stress and return to their original state when stress is removed, have been used to deliver gel-cell constructs and therapeutic agents. Here we show that a polymer-silica nanocomposite thixotropic gel can be used as a three-dimensional cell culture material. The gel liquefies when vortexed--allowing cells and biological components to be add...

Journal: :PloS one 2016
Cemal Cagatay Bilgin Gerald Fontenay Qingsu Cheng Hang Chang Ju Han Bahram Parvin

BioSig3D is a computational platform for high-content screening of three-dimensional (3D) cell culture models that are imaged in full 3D volume. It provides an end-to-end solution for designing high content screening assays, based on colony organization that is derived from segmentation of nuclei in each colony. BioSig3D also enables visualization of raw and processed 3D volumetric data for qua...

2009
Ratmir Derda Anna Laromaine Akiko Mammoto Sindy K. Y. Tang Tadanori Mammoto Donald E. Ingber George M. Whitesides

Methods. Cells and reagents We purchased MDA-MB-231 cells from ATCC and primary IMR90, HDF and primary HUVEC cells from Lonza. MDA-MB-231, IMR-90, HDF and LLC cells were cultured in Eagle’s minimal Essential medium (MEM) from Lonza supplemented with 10% fetal bovine serum (FBS) and 1% GlutaMax (both from Invitrogen). Primary HUVEC cells were cultured in endothelial growth medium (EGM-2, Lonza)....

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