CYTOO's Motility Plates to Study Cell Migration to be Launched at American Society for Cell Biology (ASCB)
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After sponsoring last year’s “World Cell Race”, showcased at ASCB 2011 with huge success, CYTOO returns to ASCB 2012 to launch a new product to study cell migration for screening applications in both oncology and drug discovery.
“The objective of the first World Cell Race was to perform a large-scale comparison of cell motility across many different adherent cell types under standardized conditions. Many contestants and laboratories over the world proposed their cells as competitors, and this collaborative competition1 demonstrated how fun and serious science can be mixed”, commented Alexandra Fuchs, COO of CYTOO.
“We were delighted to participate and design a product to make this race a success. After the World Cell Race, the success of our CYTOOchips Motility was undeniable, as they provide a perfect tool for studying cell migration, showing characteristics closer to those found in vivo². We will celebrate the first anniversary of the WCR with the launch of our CYTOOplates Motility in a standard microplate format.”
CYTOOplates Motility feature adhesive tracks of 4 different widths from 2.5 to 20 μm allowing a wide range of applications including single vs collective cell migration, and cell pairing ”, explained Constantin Nelep, Sr. Product Manager of CYTOO. “We have also seen our Motility products used in other application areas, such as directional neurite outgrowth assays.”
During ASCB 2012 meeting, CYTOO will also present the company’s 2D+ Cell Culture Platform, that was launched in July. Based on the use of adhesive micropatterns to guide cell architecture and behavior in culture, this technology contrasts with traditional 2D culture where cells spread and move in an uncontrolled manner, introducing a considerable but unnoticed variability in cell function. By defining the 2D topology of cell adhesion, 2D+ Technology enables the fine control of the spreading and 3D shape of cultured cells in single- or multi-cellular configurations, resulting in control of cell contractility, cell polarity, organelle positioning, or cell division axis.
