The Washburn Expedition of 1870, explored the region of northwestern Wyoming that a couple years later became Yellowstone National Park. Led by Henry Washburn, Nathaniel P. Langford ...
Carlos J. Bosques - Arlington MA, US Nathaniel J. Washburn - Belmont MA, US Xiangping Zhu - North Grafton MA, US Ian Christopher Parsons - Belmont MA, US
Assignee:
Momenta Pharmaceuticals, Inc. - Cambridge MA
International Classification:
G01N 24/00
US Classification:
436174, 436173, 702 19, 702 22, 702 23, 702 32
Abstract:
The present disclosure provides, among other things, methods for the identification of sulfated glycans in a mixture of glycans.
Gal Alpha 1-3Gal-Containing N-Glycans In Glycoprotein Products Derived From Cho Cells
Carlos Bosques - Arlington MA, US Jennifer Murphy - Marshfield MA, US Hetal Sarvaiya - Quincy MA, US Nathaniel Washburn - Belmont MA, US Cuihua Liu - Belmont MA, US
International Classification:
G01N 33/53 C12Q 1/02
US Classification:
435 721, 435 29
Abstract:
The present invention provides methods of evaluating CHO cells.
Antennary Fucosylation In Glycoproteins From Cho Cells
Nathaniel J. Washburn - Littleton MA, US Enrique Arevalo - Dorchester MA, US Kevin Millea - Saugus MA, US Carlos J. Bosques - Arlington MA, US Jay Duffner - Shirley MA, US Brian E. Collins - Arlington MA, US
The present invention provides methods of evaluating a glycoprotein preparation for the absence, presence or amount of an N-acetylhexosamine glycan, e.g., an N-acetylglucosamine glycan.
Gal Alpha 1-3Gal-Containing N-Glycans In Glycoprotein Products Derived From Cho Cells
- Titusville NJ, US Sucharita Roy - Acton MA, US Nathaniel Washburn - Littleton MA, US Marilyn Kehry - San Diego CA, US David J. King - Encinitas CA, US Anthony Manning - Cambridge MA, US James Meador, III - Framingham MA, US Jan Hillson - , US
International Classification:
C07K 16/28 A61P 37/02
Abstract:
The present application features antibodies that bind to human neonatal Fc receptor (FcRn). These anti-FcRn antibodies are useful, e.g., to promote clearance of autoantibodies in a subject, to suppress antigen presentation in a subject, to block an immune response, e.g., block an immune complex-based activation of the immune response in a subject, and to treat immunological diseases (e.g., autoimmune diseases) in a subject. These anti-FcRn antibodies are also useful, e.g., to decrease pathogenic antibody transport across the placenta of a pregnant subject, to increase pathogenic antibody catabolism in a pregnant subject, and to treat an antibody-mediated enhancement of viral disease in a fetus or a neonate.
- Cambridge MA, US Michael SHIFRIN - Cambridge MA, US Nathaniel J. WASHBURN - Cambridge MA, US Aneta LIWOSZ - Cambridge MA, US Nasir KHAN - Cambridge MA, US
This disclosure pertains to compositions comprising an anti-FcRn antibody, M281. The compositions include the full, intact antibody and size variants thereof that not include two antibody heavy chains and to antibody light chains. Thus, a M281 pharmaceutical composition can include: an antibody comprising a heavy chain comprising the amino acid sequence of SEQ ID NO:2 and a light chain comprising the amino acid sequence of SEQ ID NO:1, wherein the composition comprises a major protein component having a molecular weight of 140,00-145,000 Da and a minor protein component of molecular weight 118,000-120,000 Da.
- Cambridge MA, US Robin Meccariello - Brighton MA, US Jonathan C. Lansing - Reading MA, US Daniel Ortiz - Stoneham MA, US Hetal Sarvaiya - Foster City CA, US Nathaniel J. Washburn - Littleton MA, US
International Classification:
C12P 21/00 C12N 9/10 C07K 16/00 C12Q 1/48
Abstract:
Glycoproteins having particular sialylation patterns, and methods of making and using such glycoproteins, are described.