The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Oct. 17, 2017

Filed:

Jul. 30, 2012
Applicants:

Melissa K. Carpenter, Castro Valley, CA (US);

R. Scott Thies, Pleasanton, CA (US);

Inventors:

Melissa K. Carpenter, Castro Valley, CA (US);

R. Scott Thies, Pleasanton, CA (US);

Assignee:

Asterias Biotherapeutics, Inc., Fremont, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C12N 5/10 (2006.01); C12N 5/0793 (2010.01); C12R 1/91 (2006.01); C12N 5/077 (2010.01); C12Q 1/02 (2006.01); C12P 21/02 (2006.01); C12N 5/02 (2006.01); A61K 35/12 (2015.01); C12N 15/09 (2006.01); C12N 5/073 (2010.01); C12N 5/0735 (2010.01); C12N 5/079 (2010.01); C12N 15/10 (2006.01); C12N 5/07 (2010.01);
U.S. Cl.
CPC ...
C12N 5/0606 (2013.01); C12N 15/1034 (2013.01); C12N 15/1072 (2013.01); C12N 15/1096 (2013.01); A61K 35/12 (2013.01); C12N 2500/14 (2013.01); C12N 2500/30 (2013.01); C12N 2500/38 (2013.01); C12N 2500/44 (2013.01); C12N 2500/62 (2013.01); C12N 2501/105 (2013.01); C12N 2501/13 (2013.01); C12N 2501/155 (2013.01); C12N 2501/385 (2013.01); C12N 2501/39 (2013.01); C12N 2501/999 (2013.01); C12N 2502/13 (2013.01); C12N 2502/99 (2013.01); C12N 2503/02 (2013.01); C12N 2510/00 (2013.01); C12N 2510/04 (2013.01); C12N 2533/90 (2013.01);
Abstract

This invention provides a system for efficiently producing differentiated cells from pluripotent cells, such as human embryonic stem cells. Rather than permitting the cells to form embryoid bodies according to established techniques, differentiation is effected directly in monolayer culture on a suitable solid surface. The cells are either plated directly onto a differentiation-promoting surface, or grown initially on the solid surface in the absence of feeder cells and then exchanged into a medium that assists in the differentiation process. The solid surface and the culture medium can be chosen to direct differentiation down a particular pathway, generating a cell population that is remarkably uniform. The methodology is well adapted to bulk production of committed precursor and terminally differentiated cells for use in drug screening or regenerative medicine.


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