Thomas Albert - Madison WI, US Jeff Jeddeloh - Verona WI, US Bradley Swanson - Madison WI, US
International Classification:
C07H 21/04 C40B 40/06
US Classification:
506 16, 536 242
Abstract:
The present invention provides for compositions, methods and systems for targeted sequence enrichment. In particular, the present invention provides for enriching for targeted nucleic acid sequences during hybridizations in microarray assays by suppressing secondary capture of non-target nucleic acid sequences.
Methods For Directed Differentiation Of Pluripotent Stem Cells To Immune Cells
- Madison WI, US Xin ZHANG - Madison WI, US Andrew J. BRANDL - Madison WI, US Deepika RAJESH - Madison WI, US Bradley SWANSON - Madison WI, US Christie MUNN - Madison WI, US Sarah A. BURTON - Madison WI, US Wen Bo WANG - Madison WI, US
Provided herein are methods for the efficient in vitro differentiation of somatic cell-derived pluripotent stem cells to hematopoietic precursor cells, and the further differentiation of the hematopoietic precursor cells into immune cells of various myeloid or lymphoid lineages, particularly T cells, NK cells, and dendritic cells. The pluripotent cells may be maintained and differentiated under defined conditions; thus, the use of mouse feeder cells or serum is not required in certain embodiments for the differentiation of the hematopoietic precursor cells.
Methods For Directed Differentiation Of Pluripotent Stem Cells To Hla Homozygous Immune Cells
- Madison WI, US Xin ZHANG - Madison WI, US Andrew J. BRANDL - Madison WI, US Deepika RAJESH - Madison WI, US Bradley SWANSON - Madison WI, US Christie MUNN - Madison WI, US Sarah BURTON - Madison WI, US Wen Bo WANG - Madison WI, US
Assignee:
FUJIFILM Cellular Dynamics, Inc. - Madison WI
International Classification:
C12N 5/074 C12N 5/0783 C12N 5/0784 C12N 5/0789
Abstract:
Provided herein are methods for the efficient in vitro differentiation of HLA homozygous blood cell-derived pluripotent stem cells to hematopoietic precursor cells, and the further differentiation of the hematopoietic precursor cells into HLA homozygous immune cells of various myeloid or lymphoid lineages, particularly T cells, NK cells, and dendritic cells. The pluripotent cells may be maintained and differentiated under defined conditions; thus, the use of mouse feeder cells or serum is not required in certain embodiments for the differentiation of the hematopoietic precursor cells.
- Madison WI, US Xin ZHANG - Madison WI, US Andrew J. BRANDL - Madison WI, US Deepika RAJESH - Madison WI, US Bradley SWANSON - Madison WI, US Christie MUNN - Madison WI, US Sarah BURTON - Madison WI, US Wen Bo WANG - Madison WI, US Ethan McLEOD - Madison WI, US
Assignee:
FUJIFILM Cellular Dynamics, Inc. - Madison WI
International Classification:
C12N 5/0783 A61K 35/17 A61K 35/545 C07K 14/725
Abstract:
Provided herein are methods for the production of antigen-specific effector T cells and NK cells from pluripotent stem cells which express a chimeric antigen receptor (CAR). Further provided herein are methods for the adoptive cell therapy by administering the effector T cells and/or NK cells provided herein.
Methods For Directed Differentiation Of Pluripotent Stem Cells To Immune Cells
- Madison WI, US Xin ZHANG - Madison WI, US Andrew J. BRANDL - Madison WI, US Deepika RAJESH - Madison WI, US Bradley SWANSON - Madison WI, US Christie MUNN - Madison WI, US Sarah A. BURTON - Madison WI, US Wen Bo WANG - Madison WI, US
Assignee:
FUJIFILM Cellular Dynamics, Inc. - Madison WI
International Classification:
C12N 5/0783 C12N 5/0781 C12N 5/0784 C12N 15/86
Abstract:
Provided herein are methods for the efficient in vitro differentiation of somatic cell-derived pluripotent stem cells to hematopoietic precursor cells, and the further differentiation of the hematopoietic precursor cells into immune cells of various myeloid or lymphoid lineages, particularly T cells, NK cells, and dendritic cells. The pluripotent cells may be maintained and differentiated under defined conditions; thus, the use of mouse feeder cells or serum is not required in certain embodiments for the differentiation of the hematopoietic precursor cells.
Generating Mature Lineages From Induced Pluripotent Stem Cells With Mecp2 Disruption
- Madison WI, US Anne STROUSE - Madison WI, US Sarah BURTON - Madison WI, US Christie MUNN - Madison WI, US Bradley SWANSON - Madison WI, US
International Classification:
C12N 5/078 C12N 5/0783 C12N 5/071 C12N 5/079
Abstract:
Provided herein are methods for the efficient in vitro maintenance, expansion, culture, and/or differentiation of pluripotent cells with disruption of the MeCP2 gene into various erythroid, myeloid, lymphoid, or endoderm lineages, particularly mature erythrocytes. The pluripotent cells may be maintained and differentiated under defined conditions; thus, the use of mouse feeder cells or serum is not required in certain embodiments for the differentiation of the precursor cells.
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