Nicholas L. Abbott - Madison WI, US Jeffrey C. Mohr - Madison WI, US Christopher J. Murphy - Madison WI, US Elise Huang - Fitchburg WI, US Juan J. De Pablo - Madison WI, US Sean P. Palecek - Madison WI, US Nathan A. Lockwood - Minneapolis MN, US
The present invention is directed to liquid crystalline substrates useful in the culture of cells and methods of their use. In certain embodiments, the invention provides methods and devices for imaging changes (e. g. , reorganization) of extracellular matrix components by living cells.
Nicholas L. Abbott - Madison WI, US Jeffrey C. Mohr - Madison WI, US Christopher J. Murphy - Madison WI, US Elise Huang - Fitchburg WI, US Juan J. DePablo - Madison WI, US Nathan A. Lockwood - Minneapolis MN, US Sean P. Palecek - Madison WI, US
The present invention is directed to liquid crystalline substrates useful in the culture of cells and methods of their use. In certain embodiments, the invention provides methods and devices for imaging changes (e. g. , reorganization) of extracellular matrix components by living cells.
Nicholas L. Abbott - Madison WI, US Jeffrey C. Mohr - Madison WI, US Christopher J. Murphy - Madison WI, US Elise Huang - Fitchburg WI, US Juan J. DePablo - Madison WI, US Nathan A. Lockwood - Minneapolis MN, US Sean P. Palecek - Madison WI, US
The present invention is directed to liquid crystalline substrates useful in the culture of cells and methods of their use. In certain embodiments, the invention provides methods and devices for imaging changes (e. g. , reorganization) of extracellular matrix components by living cells.
Sean Palecek - Verona WI, US Jeffrey Mohr - Madison WI, US Juan De Pablo - Madison WI, US
International Classification:
C12N 5/02 C12M 1/16 C12N 5/08
US Classification:
435366000, 435287900, 435374000, 435395000
Abstract:
A three-dimensional microwell system that supports long term embryonic stem cell (ESCs) culture and formation of homogeneous embryoid bodies (EBs) is described. Microwell-cultured ESCs remain viable and undifferentiated for several weeks in culture and maintain undifferentiated replication when passaged to Matrigel-coated, tissue culture-treated polystyrene dishes. Microwell-cultured ESCs maintain pluripotency, differentiating to each of the three embryonic germ layers. ESC aggregates released from microwells can be passaged for undifferentiated replication or differentiated to monodisperse EBs. The ability to constrain ESC growth in three dimensions advantageously provides for more efficient, reproducible culture of undifferentiated cells, high-throughput screening, and the ability to direct ESC differentiation by generating monodisperse EBs of a desired size and shape.
Cryopreservation Of Human Embryonic Stem Cells In Microwells
Sean P. Palecek - Madison WI, US Juan J. DePablo - Madison WI, US Jeffrey C. Mohr - Madison WI, US Lin Ji - Madison WI, US
International Classification:
C12N 5/06 C12M 1/00
US Classification:
435374, 4353071
Abstract:
The present invention relates to methods and structures for preparing stem cells for use in cryopreservation methods. Stem cell colonies are provided between first and second matrix portions and are exposed to a carbohydrate-containing cryoprotecting medium and a freezing medium. The methods of the invention yield cryopreserved cells that maintain cell viability and exhibit limited cell differentiation after freezing and thawing, facilitating storage, shipping and handling of embryonic stem cell stocks and lines for research and therapeutics.
Timothy J. Kamp - Madison WI, US Jianhua Zhang - Madison WI, US Jeffrey C. Mohr - Glenview IL, US Juan J. Depablo - Madison WI, US Sean P. Palecek - Verona WI, US
International Classification:
C12N 5/071 C12N 5/02 C12N 5/00 C40B 40/14
US Classification:
435366, 435377, 435325, 506 20, 435374
Abstract:
A three-dimensional microwell system that supports long term pluripotent cell culture and formation of homogeneous embryoid bodies (EBs) is described. Microwell-cultured pluripotent cells remain viable and undifferentiated for several weeks in culture and maintain undifferentiated replication when passaged to Matrigel-coated, tissue culture-treated polystyrene dishes. Microwell-cultured pluripotent cells maintain pluripotency, differentiating to each of the three embryonic germ layers. Pluripotent cell aggregates released from microwells can be passaged for undifferentiated replication or differentiated to monodisperse EBs. The ability to constrain pluripotent cell growth in three dimensions advantageously provides for more efficient, reproducible culture of undifferentiated cells, high-throughput screening, and the ability to direct pluripotent cell differentiation by generating monodisperse EBs of a desired size and shape. Cardiomyocyte-rich EBs are obtained from pluripotent cells cultured in microwells of defined size and shape.
Booz & Company - Greater Chicago Area since Mar 2011
Senior Associate (Engagement Manager)
Booz & Company - Greater Chicago Area Jan 2008 - Mar 2011
Associate
University of Wisconsin-Madison - Madison, Wisconsin Area Jun 2002 - Dec 2007
Research Assistant / PhD Candidate
Education:
University of Wisconsin-Madison 2002 - 2007
PhD, Chemical & Biological Engineering
University of Idaho 1998 - 2002
BS, Chemical Engineering
Skills:
Management Consulting Strategy Organizational Design Corporate Development Business Strategy Strategic Consulting Business Transformation Acquisition Integration Program Management Operational Excellence Benchmarking Due Diligence Pricing Strategy Go To Market Strategy Consumer Products Healthcare Health Insurance Hospital Consulting Cost Management Cost Engineering Operations Management